FDA UDI Not in Commercial Distribution 🇺🇸 United States

SilveRest™

DI: 10009336008459 · Model: A10022 · GRAPHIC CONTROLS ACQUISITION CORP
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
SilveRest™
Primary DI
10009336008459
Version / Model
A10022
Catalog Number
A10022-J(100)
Company Name
GRAPHIC CONTROLS ACQUISITION CORP
Labeler DUNS
002111896
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2017-07-13
Public Version
3
Public Version Date
2023-12-19
Public Version Status
Update
Public Device Record Key
eff81a40-e3a1-4022-8bc8-9d639a2585c8
Distribution End Date
2023-12-18

Device Description

Resting ECG TAB 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
Primary 10009336008459
Package 30009336008453
Package 50009336008457
Unit of Use 00009336008452

Customer Contacts

Phone
800-669-6905