FDA UDI Not in Commercial Distribution 🇺🇸 United States

Vermed

DI: 10009336008442 · Model: V8930 · GRAPHIC CONTROLS ACQUISITION CORP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
30

Basic Information

Brand Name
Vermed
Primary DI
10009336008442
Version / Model
V8930
Catalog Number
V8930
Company Name
GRAPHIC CONTROLS ACQUISITION CORP
Labeler DUNS
002111896
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2017-07-12
Public Version
3
Public Version Date
2019-02-13
Public Version Status
Update
Public Device Record Key
3f1e2a03-cd67-49a0-a688-c25c77b88a42
Distribution End Date
2019-02-12

Device Description

ECG Monitoring Electrodes

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 50009336008440
Primary 10009336008442
Unit of Use 00009336008445

Customer Contacts

Phone
800-669-6905