Liverty 306466

by Suzhou BD Medical Device Co., Ltd

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00382903064663 UDI-DI	Date9 Jun 2022Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Liverty
Generic Name: Soft-tissue biopsy procedure kit, non-medicated
Model / Ref / Catalog: 306466

Primary DI / UDI-DI: 00382903064663
510(k) Number: K221440
FDA Product Code: DYB
GMDN Term: Soft-tissue biopsy procedure kit, non-medicated

Device Class: Class II
Regulation Number: 870.1340
GUDID distribution status: In Commercial Distribution

Properties

Sterile
Single Use
Prescription Use
Convenience Kit
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (7)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No