SilveRest™ A10022-J(100)

GUDID 10009336008459

Electrocardiographic electrode, single-use

Primary Device ID	10009336008459
NIH Device Record Key	eff81a40-e3a1-4022-8bc8-9d639a2585c8
Commercial Distribution Discontinuation	2023-12-18
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	SilveRest™
Version Model Number	A10022
Catalog Number	A10022-J(100)
Company DUNS	002111896
Company Name	GRAPHIC CONTROLS ACQUISITION CORP
Device Count	100
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00009336008452 [Unit of Use]
GS1	10009336008459 [Primary]
GS1	30009336008453 [Package] Package: [10 Units] Discontinued: 2023-12-18 Not in Commercial Distribution
GS1	50009336008457 [Package] Contains: 30009336008453 Package: [4 Units] Discontinued: 2023-12-18 Not in Commercial Distribution

DRX	Electrode, Electrocardiograph

Steralize Prior To Use	false
Device Is Sterile	false

Mark Image Registration \| Serial	Company Trademark Application Date
SILVEREST 74257695 1739637 Dead/Cancelled	VERMONT MEDICAL, INC. 1992-03-23