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Quinelato QD.342.03

by Schobell Industrial Ltda

Quinelato QD.342.03 is a Class I device made by Schobell Industrial Ltda, listed in FDA GUDID since 10 Jan 2023 (UDI-DI 07898506854714), 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 Number07898506854714 UDI-DI Date10 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  • Withdrawn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
Quinelato
Generic name
Periotome, reusable
Model / Ref / Catalog
QD.342.03
Primary DI / UDI-DI
07898506854714
FDA product code
EML
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periotome, reusable

Other devices from Schobell Industrial Ltda

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Properties

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