Trucleartm 72203618

by Smith & Nephew, Inc.

Trucleartm 72203618 is a Class II device made by Smith & Nephew, Inc., listed in FDA GUDID since 21 Sep 2015 (UDI-DI 00885554030549), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00885554030549 UDI-DI	Date21 Sep 2015Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00885554030549

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Trucleartm
Generic name: Arthroscopic obturator
Model / Ref / Catalog: 72203618
Description: TRUCLEAR UNIVERSAL OP. HYST. STOPCOCK SE

Primary DI / UDI-DI: 00885554030549
FDA product code: HIH
GMDN term: Arthroscopic obturator

Device class: Class II
Regulation number: 884.1690
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use

Other properties (13, all answered No)