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Safety-Lancet Super

FDA UDI

Class II (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
Safety-Lancet Super FDA UDI
Generic Name
Manual blood lancing device, single-use FDA UDI
Model / Reference
85.1018 FDA UDI

Identifiers

Catalog Number
85.1018 FDA UDI
Primary DI / UDI-DI
04038917085052 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Manual blood lancing device, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual blood lancing device, single-use

Safety-Lancet Super by Sarstedt Aktiengesellschaft & Co.KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual blood lancing device, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI daa17769-554b-4a88-befa-8710d095aa4a 34 fields · synced May 30, 2026