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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 transfer tube IVD, clot activator FDA UDI
Device Name
BD Vacutainer®,Citrate,13x75mm,1.8mL PK100 FDA UDI
Model / Reference
34673 FDA UDI
Description
BD Vacutainer®,Citrate,13x75mm,1.8mL PK100 FDA UDI

Identifiers

Catalog Number
34673 FDA UDI
Primary DI / UDI-DI
00817517020304 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Capillary blood transfer tube IVD, clot activator 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

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: Capillary blood transfer tube IVD, clot activator

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

Similar devices

Also classified as Capillary blood transfer tube IVD, clot activator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI a40b487f-a1b2-4193-987e-5db0dbaa9198 35 fields · synced Jun 1, 2026