FDA UDI In Commercial Distribution 🇺🇸 United States

Vermed

DI: 50813150021611 · Model: A10091-30 · GRAPHIC CONTROLS ACQUISITION CORP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
30

Basic Information

Brand Name
Vermed
Primary DI
50813150021611
Version / Model
A10091-30
Catalog Number
A10091-30
Company Name
GRAPHIC CONTROLS ACQUISITION CORP
Labeler DUNS
002111896
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2017-02-17
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8e038703-2184-433c-8e9c-829c0818a56e

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 60813150021618
Primary 50813150021611
Unit of Use 00813150021616

Customer Contacts