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Princeton 71715-08

by Princeton Medical Group, Inc.

Princeton 71715-08 is a Class I device made by Princeton Medical Group, Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI 00810238290179), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810238290179 UDI-DI Date29 Oct 2026ListedStatusListed 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  • Withdrawn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
Princeton
Generic name
Intrauterine curette, manual
Model / reference
71715-08
Primary DI / UDI-DI
00810238290179
FDA product code
FZS
GMDN term
Intrauterine curette, manual
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Princeton Medical Group, Inc.

See all devices from Princeton Medical Group, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)