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Allomap Specimen Collection Kit

FDA UDI

Class I (US FDA UDI)

by Caredx, Inc.

Identity

Trade Name
Allomap Specimen Collection Kit FDA UDI
Generic Name
Phlebotomy kit FDA UDI
Device Name
Convenience Kit for Phlebotomy of blood sample for AlloMap testing FDA UDI
Model / Reference
HTx-00007 FDA UDI
Description
Convenience Kit for Phlebotomy of blood sample for AlloMap testing FDA UDI

Identifiers

Primary DI / UDI-DI
00860193001716 FDA UDI
FDA Product Code
OFZ FDA UDI
GMDN Term
Phlebotomy kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1100 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phlebotomy kit

Allomap Specimen Collection Kit by Caredx, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phlebotomy kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caredx, Inc.

Sources (1)

  • FDA UDI d01faf38-83bf-42d2-8ce9-bb06a7094a91 35 fields · synced May 30, 2026