← Back to catalogue

Haemolance Plus, safety lancet

FDA UDI

Class II (US FDA UDI)

by Htl Strefa S A

Identity

Trade Name
Haemolance Plus, safety lancet FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Safety lancets are sterile, single use medical devices intended for capillary blood sampling. FDA UDI
Model / Reference
Low Flow, 25G 1.4mm FDA UDI
Description
Safety lancets are sterile, single use medical devices intended for capillary blood sampling. FDA UDI

Identifiers

Catalog Number
7371 FDA UDI
Primary DI / UDI-DI
05907506237426 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

No

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

Haemolance Plus, safety lancet by Htl Strefa S A — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Htl Strefa S A

Sources (1)

  • FDA UDI 28a9b689-b170-44c7-a6d4-07fad6f94b69 35 fields · synced May 30, 2026