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PremierPro 6330

by Prestige Ameritech

PremierPro 6330 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 2 Aug 2020 (UDI-DI 00818566010254), 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 Number00818566010254 UDI-DI Date2 Aug 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  • Withdrawn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
Mechanical external stethoscope
Model / Ref / Catalog
6330
Primary DI / UDI-DI
00818566010254
FDA product code
LDE
GMDN term
Mechanical external stethoscope
Device class
Class I
Regulation number
870.1875
GUDID distribution status
In Commercial Distribution
Size
Length — 30 Inch

Related devices

Category: Mechanical external stethoscope

Similar devices in this category

Other devices filed under Mechanical external stethoscope.

Other devices from Prestige Ameritech

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Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)