N/M Ldc

by Shandong Lianfa Medical Plastic Products CO., LTD 2 variants

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	Number06949517009462 UDI-DI	Date10 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Withdrawn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: N/M
Generic Name: Manual blood lancing device, reusable
Model / Reference: LDC

Primary DI / UDI-DI: 06949517009462
FDA Product Code: QRK
GMDN Term: Manual blood lancing device, reusable

Device Class: Class II
Regulation Number: 878.4850
GUDID distribution status: In Commercial Distribution

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See all devices from Shandong Lianfa Medical Plastic Products Co., Ltd. →

Properties

Premarket Exempt
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (10)

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