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Sterilance soft twist lancet

FDA UDI

Class II (US FDA UDI)

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
Sterilance soft twist lancet FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Sterilance soft twist lancet,33G,100Lancets/box FDA UDI
Model / Reference
01-0133 FDA UDI
Description
Sterilance soft twist lancet,33G,100Lancets/box FDA UDI

Identifiers

Primary DI / UDI-DI
16945630108744 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Blood lancet, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood lancet, single-use

Sterilance soft twist lancet by Sterilance Medical (Suzhou) Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3646c425-a088-4200-84c0-b83aece95421 33 fields · synced May 31, 2026