Skip to content

CarbonMed CMBNA/1820

by Carbon (Shenzhen) Medical Device Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974405095067 UDI-DI Date25 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
CarbonMed
Generic Name
Side-notch biopsy gun handpiece/needle
Model / Reference
CMBNA/1820
Primary DI / UDI-DI
06974405095067
510(k) Number
FDA Product Code
KNW
GMDN Term
Side-notch biopsy gun handpiece/needle
Device Class
Class II
Regulation Number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K243296)

Other devices from Carbon (Shenzhen) Medical Device Co., Ltd.

See all devices from Carbon (Shenzhen) Medical Device Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No