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Marketlab Inc

FDA UDI

Class II (US FDA UDI)

by Marketlab Inc.

Identity

Trade Name
Marketlab Inc FDA UDI
Generic Name
General-purpose syringe/needle FDA UDI
Device Name
3ml Syringe 21x1-1/2 Safety Needle Combo - 50PK FDA UDI
Model / Reference
6156 FDA UDI
Description
3ml Syringe 21x1-1/2 Safety Needle Combo - 50PK FDA UDI

Identifiers

Catalog Number
6156 FDA UDI
Primary DI / UDI-DI
00817517020632 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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: General-purpose syringe/needle

Marketlab Inc by Marketlab Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI 9622a4a9-147e-4406-9634-6cf877b28b3d 35 fields · synced May 30, 2026