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Medlance Plus, safety lancet

FDA UDI

Class II (US FDA UDI)

by Htl Strefa S A

Identity

Trade Name
Medlance Plus, safety lancet FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Sterile,single-use safety lancets for capillary blood sampling. FDA UDI
Model / Reference
Extra, 21G 2.4 mm FDA UDI
Description
Sterile,single-use safety lancets for capillary blood sampling. FDA UDI

Identifiers

Catalog Number
7045 FDA UDI
Primary DI / UDI-DI
05907506237129 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

Yes

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

Medlance 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

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Manufacturer

Manufacturer
Htl Strefa S A

Sources (1)

  • FDA UDI 8c1f1460-d8b3-4329-976a-d382e03343bc 35 fields · synced Jun 6, 2026