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A. Titan Instruments P 302

by A.Titan Instruments

A. Titan Instruments P 302 is a Class I device made by A.Titan Instruments, listed in FDA GUDID since 12 Jan 2023 (UDI-DI 00841685104795), 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 Number00841685104795 UDI-DI Date12 Jan 2023ListedStatusListed 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  • Withdrawn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
A. Titan Instruments
Generic name
Periotome, reusable
Model / reference
P 302
Primary DI / UDI-DI
00841685104795
FDA product code
DZN
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization

Related devices

Category: Periotome, reusable

Other devices from A.Titan Instruments

See all devices from A.Titan Instruments →

Properties

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