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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
Capillary blood collection tube IVD, lithium heparin FDA UDI
Device Name
Lithium Heparin Capillary Collection-200ul 50/pk. FDA UDI
Model / Reference
5601 FDA UDI
Description
Lithium Heparin Capillary Collection-200ul 50/pk. FDA UDI

Identifiers

Catalog Number
5601 FDA UDI
Primary DI / UDI-DI
00817517020496 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Capillary blood collection tube IVD, lithium heparin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Capillary blood collection tube IVD, lithium heparin

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

Similar devices

Also classified as Capillary blood collection tube IVD, lithium heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI eadb7238-ac2d-4b44-af08-debd0d3d1f0a 35 fields · synced Jun 8, 2026