← Back to catalogue

PremierPro

FDA UDI

Class II (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Pressure Lancet, 26g, 1.8mm-D, Sterile, Yellow, 100/bx FDA UDI
Model / Reference
7503 FDA UDI
Description
Pressure Lancet, 26g, 1.8mm-D, Sterile, Yellow, 100/bx FDA UDI

Identifiers

Catalog Number
7503 FDA UDI
Primary DI / UDI-DI
00818566013644 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood lancet, single-use

PremierPro by Svs Llc — 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
Svs Llc

Sources (1)

  • FDA UDI 7937d070-99f6-49f6-b2a8-fe21fbc699eb 35 fields · synced May 30, 2026