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PremierPro 6253

by Prestige Ameritech

PremierPro 6253 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 3 Sep 2020 (UDI-DI 00818566019394), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00818566019394 UDI-DI Date3 Sep 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  • Withdrawn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
Rigid intubation laryngoscope, single-use
Model / Ref / Catalog
6253
Primary DI / UDI-DI
00818566019394
FDA product code
CCW
GMDN term
Rigid intubation laryngoscope, single-use
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid intubation laryngoscope, single-use

Similar devices in this category

Other devices filed under Rigid intubation laryngoscope, single-use.

Other devices from Prestige Ameritech

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)