Biopsy pipettes S-P-B35.30

by Guangzhou Pinzhi Medical Device Co., Ltd.

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

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06972598791865 UDI-DI	Date15 Dec 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Biopsy pipettes
Generic Name: User-induced micropipette
Model / Reference: S-P-B35.30

Primary DI / UDI-DI: 06972598791865
FDA Product Code: PUC
GMDN Term: User-induced micropipette

Device Class: Class II
Regulation Number: 884.6130
GUDID distribution status: In Commercial Distribution

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See all devices from Guangzhou Pinzhi Medical Device Co., Ltd. →

Properties

Sterile
Single Use
Prescription Use
Premarket Exempt
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (7)

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