velvet XP 200 TTNF202

GUDID 00841277108903

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Primary Device ID	00841277108903
NIH Device Record Key	175c2254-e5a3-4510-8f6c-3bf9171f4632
Commercial Distribution Discontinuation	2024-11-15
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	velvet XP 200
Version Model Number	TTNF202
Catalog Number	TTNF202
Company DUNS	004072158
Company Name	SEMPERMED USA, INC.
Device Count	200
DM Exempt	false
Pre-market Exempt	false
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	false
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00841277108859 [Primary]
GS1	00841277108903 [Unit of Use]

LZA	Polymer Patient Examination Glove

Steralize Prior To Use	false
Device Is Sterile	false

00841277108934	velvet XP 200 Nitrile Exam Glove PF, size XL
00841277108927	velvet XP 200 Nitrile Exam Glove PF, size L
00841277108910	velvet XP 200 Nitrile Exam Glove PF, size M
00841277108903	velvet XP 200 Nitrile Exam Glove PF, size S
00841277108897	velvet XP 200 Nitrile Exam Glove PF, size XS