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One +Step

FDA UDI

Class II (US FDA UDI)

by Shandong Lianfa Medical Plastic Products CO., LTD

Identity

Trade Name
One +Step FDA UDI
Generic Name
Manual blood lancing device, reusable FDA UDI
Device Name
A convenience kit consisting of 1 One Step Lancing Device and 100 pcs 23g lancets FDA UDI
Model / Reference
LDE FDA UDI
Description
A convenience kit consisting of 1 One Step Lancing Device and 100 pcs 23g lancets FDA UDI

Identifiers

Primary DI / UDI-DI
06949517009028 FDA UDI
510(k) Number
K222472 FDA UDI
FDA Product Code
QRL FDA UDI
GMDN Term
Manual blood lancing device, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood lancet, single-useManual blood lancing device, reusable

One +Step by Shandong Lianfa Medical Plastic Products CO., LTD — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual blood lancing device, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 320e73aa-01c9-4410-9e6d-b06250a1d523 34 fields · synced May 30, 2026