Preventi PRB2240

by Rushmedics LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00850046528101 UDI-DI	Date12 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Preventi
Generic Name: Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / Ref / Catalog: PRB2240

Primary DI / UDI-DI: 00850046528101
FDA Product Code: LZA, LZC, QDO
GMDN Term: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Device Class: Class I
Regulation Number: 880.6250
GUDID distribution status: In Commercial Distribution

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Properties

Single Use
Lot / Batch Number
Manufacturing Date

Other properties (11)

Sterile: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No