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Trocar T060434

by Adria SRL

Trocar T060434 is a Class I device made by Adria SRL, listed in FDA GUDID since 13 Aug 2024 (UDI-DI 08033737117576), 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 Number08033737117576 UDI-DI Date13 Aug 2024ListedStatusListed 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  • Withdrawn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
Trocar
Generic name
Vertebral bone biopsy procedure kit, single-use
Model / reference
T060434
Primary DI / UDI-DI
08033737117576
FDA product code
GAA
GMDN term
Vertebral bone biopsy procedure kit, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Vertebral bone biopsy procedure kit, single-use

Similar devices

Other devices filed under FDA product code GAA (Needle, Aspiration And Injection, Disposable).

Other devices from Adria SRL

See all devices from Adria SRL →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)