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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
Blood collection set, invasive FDA UDI
Device Name
SampLok® Adapter Cap 3 Insert for 42829 PK65 FDA UDI
Model / Reference
42830 FDA UDI
Description
SampLok® Adapter Cap 3 Insert for 42829 PK65 FDA UDI

Identifiers

Catalog Number
42830 FDA UDI
Primary DI / UDI-DI
00817517020403 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Blood collection set, invasive 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood collection set, invasive

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

Similar devices

Also classified as Blood collection set, invasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI f2f5d8f1-f270-4f79-aa82-ab4e99b3ef45 35 fields · synced Jun 1, 2026