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Thd Biopsy (Gi - Xl)

by Thd SpA

Thd Biopsy (Gi - Xl) (800328) is a Class I device made by Thd SpA, listed in FDA GUDID since 20 Feb 2025 (UDI-DI 08051887047413), 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 Number08051887047413 UDI-DI Date20 Feb 2025ListedStatusListed 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  • Withdrawn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
Thd Biopsy
Generic name
Rigid endoscopic biopsy forceps, single-use
Model / Ref / Catalog
THD BIOPSY (GI - XL), 800328
Primary DI / UDI-DI
08051887047413
FDA product code
FCL
GMDN term
Rigid endoscopic biopsy forceps, single-use
Device class
Class I
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution
Size
Length — 34 Centimeter

Similar devices

Other devices filed under FDA product code FCL (Forceps, Biopsy, Non-Electric).

Other devices from Thd SpA

See all devices from Thd SpA →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)