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Paul Banditt RETWIED0

by Terlain Enterprises, Inc.

Paul Banditt RETWIED0 is a Class I device made by Terlain Enterprises, Inc., listed in FDA GUDID since 25 Sep 2026 (UDI-DI D955RETWIED01), 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 NumberD955RETWIED01 UDI-DI Date25 Sep 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Paul Banditt
Generic name
Hand-held dental retractor
Model / reference
RETWIED0
Primary DI / UDI-DI
D955RETWIED01
FDA product code
EIF
GMDN term
Hand-held dental retractor
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Terlain Enterprises, Inc.

See all devices from Terlain Enterprises, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)