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Bone Marrow Kit

FDA UDI

Class I (US FDA UDI)

by Medical Chemical Corporation

Identity

Trade Name
Bone Marrow Kit FDA UDI
Generic Name
Evacuated blood collection tube IVD, K2EDTA FDA UDI
Device Name
A kit for collection and transport of blood specimens. FDA UDI
Model / Reference
4505K FDA UDI
Description
A kit for collection and transport of blood specimens. FDA UDI

Identifiers

Catalog Number
4505K FDA UDI
Primary DI / UDI-DI
M4456508K1 FDA UDI
FDA Product Code
KDT FDA UDI
JKA FDA UDI
GMDN Term
Evacuated blood collection tube IVD, K2EDTA FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Evacuated blood collection tube IVD, K2EDTA

Bone Marrow Kit by Medical Chemical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evacuated blood collection tube IVD, K2EDTA.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Chemical Corporation

Sources (1)

  • FDA UDI 04a09fdf-186b-4df6-a5dc-ff4f097b5580 35 fields · synced Jun 9, 2026