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Quinelato QO.397.22

by Schobell Industrial Ltda

Quinelato QO.397.22 is a Class I device made by Schobell Industrial Ltda, listed in FDA GUDID since 16 Dec 2022 (UDI-DI 07898506848621), 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 Number07898506848621 UDI-DI Date16 Dec 2022ListedStatusListed 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  • Withdrawn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
Quinelato
Generic name
Bone holding forceps
Model / Ref / Catalog
QO.397.22
Primary DI / UDI-DI
07898506848621
FDA product code
LXH
GMDN term
Bone holding forceps
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone holding forceps

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Other devices filed under Bone holding forceps.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)