← Back to catalogue

PremierPro Lancet

FDA UDI

Class II (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro Lancet FDA UDI
Generic Name
Blood collection tube holder/needle FDA UDI
Device Name
Luer Lock Access Device, Sterile FDA UDI
Model / Reference
7580 FDA UDI
Description
Luer Lock Access Device, Sterile FDA UDI

Identifiers

Catalog Number
7580 FDA UDI
Primary DI / UDI-DI
00811220033378 FDA UDI
510(k) Number
K172763 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Blood collection tube holder/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

Yes

FDA UDI

Category: Blood collection tube holder/needle

PremierPro Lancet by Svs Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood collection tube holder/needle.

Cleared under the same submission

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 b02cbba1-2c71-4095-a517-58aa4e537aba 36 fields · synced May 31, 2026