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PremierPro 2141

by Prestige Ameritech

PremierPro 2141 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 25 Jul 2020 (UDI-DI 00854344002776), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854344002776 UDI-DI Date25 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
PremierPro
Generic name
Surgical cap, single-use
Model / Ref / Catalog
2141
Primary DI / UDI-DI
00854344002776
FDA product code
FYF
GMDN term
Surgical cap, single-use
Device class
Class I
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical cap, single-use

Similar devices

Other devices filed under FDA product code FYF (Cap, Surgical).

Other devices from Prestige Ameritech

See all devices from Prestige Ameritech →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)