Medical Device Adverse Event Reporting Form: Materiovigilance Programme of India (Mvpi)

MEDICAL DEVICE ADVERSE EVENT REPORTING FORM
Materiovigilance Programme of India (MvPI)

This form is intended to collect information on Medical Devices Adverse Event in India. The form is designed to be used voluntarily by
Manufacturer/Importer/Distributor of Medical Devices, Healthcare Professionals and anyone with direct/indirect knowledge of Medical
Devices Adverse Event.
General Information
1. Date of Report :
2. Type of Report : Initial  Follow up  Final  Trend 
3. Reporter Reference for MDMC only:  Centre  Location  Month-Year  Case No.
Reporter Details
1. Type of Reporter : (a) Manufacturer  (b) Importer  (c) Distributor  (d) Healthcare Professional 
(e) Patient  (f) Others  specify ........................................................
2. In case, where the reporter is not manufacturer, fill the following details: -
(a) Has the reporter informed the incident to the manufacturer?
Yes  No 
(b) Is the reporter also submitting the report on behalf of the manufacturer?
Yes  No 
3. Reporter contact information:
a) Name :
b) Address :
c) Tel. /Mobile :
d) Email :
Device Category
Medical Device In Vitro Diagnostics (IVD) Medical Equipments / Machines
I. Therapeutic  Diagnostic  I. Kits  I. Therapeutic  Diagnostic 

Both  Preventive  II. Reagents  II. Therapeutic & Diagnostic 
Assistive  III. Calibrator  III. Preventive 
II. Implantable device  IV. Control Material  IV. Assistive 
Non-Implantable device  V. Others  V. Imaging 
III. Invasive  Non-Invasive  VI. IVD electronic reader/  VI. Invasive  Non-Invasive 
IV. Single use device  Analyzer VII. Others 
Reusable device 
Reuse of manufacture marked
Single use device 
V. Sterile  Non Sterile 
VI. Personal use / Homecare use 
Instruction for use Section A-F

 If Medical Devices/Equipments/Machines : Please fill all the sections i.e. A, B, C, D, E & F
 If in Vitro Diagnostics (IVD) : Please fill sections i.e. A (except 6, 7, 8, 13, 14 & 16), B (except 1, 2, 6 & 8), D, E, & F

(A) Device Details
Device Name / Trade Name / Brand Name: ……………………………………………………………………………………….
Details Name Address
Manufacturer
Importer
Distributor
1. a) Is the device notified/regulated in India : Yes  No 
b) Device Risk Classification as per India MDR 2017 : A  B  C  D 

2. License No. (Manufacture/Import) :
3. Catalogue No. :
4. Model No. :
5. Lot / Batch No. :
6. Serial No. :
7. Software Version :
8. Associated Devices / Accessories :
9. Nomenclature Code if applicable; GMDN/UMDNS :
10. UDI No. (If applicable) :
11. Installation Date :
12. Expiration Date :
13. Last preventive maintenance date (dd/mm/yyyy) :
14. Last calibration date (dd/mm/yyyy) :
15. Year of manufacturing :
16. How long was device/Equipment/Machine in use :
17. Availability of device for evaluation : Yes  No 

If no, was the device destroyed  Still in use  return to manufacturer or importer/distributor 
18. Is the usage of device as per manufacturer claim /Instruction for use/user manual: Yes  No 
If no specify usage ………………………………………………………………………………………………………..…..
………………………………………………………………………………………………………………………………..….
19. For devices not regulated / notified in India : Regulator / Regulatory status in country of origin
…………………………………………………………………………
(B) Event Description
1. Date of Event / Near miss incident: 7. Serious event: 

2. Date of Implant/Explant (If applicable): If serious, Tick the appropriate reason
3. Location of Event: a) Death (DD/MM/YY)  …..….…/…..….…/…..….…
Hospital Premise  Manufacture/Distributor premise  b) Life Threatening 
Home  Others  c) Disability or permanent damage 
4. Device Operator:-
d) Hospitalization 
Healthcare Professional  Patient  Others 
e) Congenital anomaly /birth defect  
Problem noted prior to use/near miss event  f) Any other serious (Imp. medical event) 
5. Device disposition / Current location:
g) Required intervention to prevent / permanent 
a) Returned to company  If yes, date ……/……. /….…
Impairment / damage device
b) Remains implanted in patient  8. Non serious event 
c) Within the healthcare facility  9. Whether other medical devices were used at same time
d) At patient home  with above device if yes, please specify name(s)/use(s)
e) Destroyed  …………………………………………………………………………………
…………………………………………………………………………………
f) Others (specify) 
…………………………………………………………………………………
6. Is device in use after incidence : Yes  No 
10. Detail description of Event:-
For manufacturer/authorized representative use only
11. Frequency of occurrence of Year No. of Similar Total No. Frequency of Occurrence
similar Adverse Event in India in Adverse Events Supplied (%)
past 3 years
12. Frequency of occurrence of Year No. of Similar Total No. Frequency of Occurrence
similar Adverse Event in globally Adverse Events Supplied (%)
in past 3 years
(C) Patient Information, History & Outcome
1. Patient Hospital ID : 7. Patient Outcomes:

2. Patient Initial : a) Recovered Date (DD/MM/YY)  ……/……./….…
3. Age : b) Not yet recovered 
4. Gender : Male  Female  Others  c) Death  (DD/MM/YY)  ……/……./….…
5. Weight :
d) Others 
6. Other relevant history, including pre-existing medical
Please specify……….……………………………………………..…
conditions…………………………………………………………………………
……………………………………………………………………………………..…
……………………………………………………………………………………..…
……………………………………………………………………………………..…
……………………………………………………………………………………..…
……………………………………………………………………………………..…
………………………………………………………………………………………
…………………………………………………………………………………………
……………………………………………………………………………………..…
…………………………………………………………………………………..…..
(D) Healthcare Facility Information (if available)
1. Name :
2. Address :
3. Contact Person Name at the site of event :
4. Tel. No. :
5. Email :
(E) Causality Assessment
1. Investigation action taken:
2. Root cause of problem (Applicable for follow up / final reports):
(F) Manufacturer/Authorized Representative Investigation & Action taken

1. Manufacturer/Authorized Representative device risk analysis report:
2. Corrective / preventive action taken:
3. Device history review:
Where to report?
Duly filled Medical Device Adverse Event Reporting Form can be sent to Indian Pharmacopoeia Commission, Ministry of Health and
Family Welfare, Government of India, Sector-23, Rajnagar, Ghaziabad-20002, Tel-0120-2783400, 2783401 and 2783392, FAX:0120-
2783311 or email to mvpi.ipcindia@gmail.com Or Call on Helpline no. 1800 180 3024 to report Adverse event.
Partnering
Organizations
Disclaimer
Confidentiality: The patient’s identity is held in strict confidence and protected to the fullest extent. Programme staff is not expected to and will not disclose the
reporter’s identity in response to a request from the public. Submission of a report does not constitute an admission that me dical personnel or manufacturer or
the product caused or contributed to the adverse even t.

Medical Device Adverse Event Reporting Form: Materiovigilance Programme of India (Mvpi)

Uploaded by

Copyright:

Available Formats

Medical Device Adverse Event Reporting Form: Materiovigilance Programme of India (Mvpi)

Uploaded by

Document Information

Original Description:

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Medical Device Adverse Event Reporting Form: Materiovigilance Programme of India (Mvpi)

Uploaded by

Copyright:

Available Formats

MEDICAL DEVICE ADVERSE EVENT REPORTING FORM

Materiovigilance Programme of India (MvPI)

I. Therapeutic  Diagnostic  I. Kits  I. Therapeutic  Diagnostic 

Instruction for use Section A-F

Device Name / Trade Name / Brand Name: ……………………………………………………………………………………….

Details Name Address

1. a) Is the device notified/regulated in India : Yes  No 

b) Device Risk Classification as per India MDR 2017 : A  B  C  D 

5. Lot / Batch No. :

8. Associated Devices / Accessories :

9. Nomenclature Code if applicable; GMDN/UMDNS :

10. UDI No. (If applicable) :

11. Installation Date :

12. Expiration Date :

13. Last preventive maintenance date (dd/mm/yyyy) :

14. Last calibration date (dd/mm/yyyy) :

15. Year of manufacturing :

16. How long was device/Equipment/Machine in use :

17. Availability of device for evaluation : Yes  No 

1. Date of Event / Near miss incident: 7. Serious event: 

10. Detail description of Event:-

For manufacturer/authorized representative use only

(C) Patient Information, History & Outcome

1. Patient Hospital ID : 7. Patient Outcomes:

1. Investigation action taken:

2. Root cause of problem (Applicable for follow up / final reports):

(F) Manufacturer/Authorized Representative Investigation & Action taken

2. Corrective / preventive action taken:

3. Device history review:

You might also like