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Ohki Baum 30-0101

by Charmant Inc.

Ohki Baum 30-0101 is a Class I device made by Charmant Inc., listed in FDA GUDID since 18 Sep 2023 (UDI-DI 00883475950014), 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 Number00883475950014 UDI-DI Date18 Sep 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  • Withdrawn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
Ohki Baum
Generic name
Vascular scissors
Model / reference
30-0101
Primary DI / UDI-DI
00883475950014
FDA product code
DWS
GMDN term
Vascular scissors
Device class
Class I
Regulation number
870.4500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code DWS (Instruments, Surgical, Cardiovascular).

Other devices from Charmant Inc.

See all devices from Charmant Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)