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BD Vacutainer® CPT™ Cell Preparation Tube with Sodium Heparin

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® CPT™ Cell Preparation Tube with Sodium Heparin FDA UDI
Generic Name
Evacuated blood collection tube IVD, anticoagulant/separator/density solution FDA UDI
Device Name
TUBE CPTHEP GC 16X125 8.0 MLBL RD/GN FDA UDI
Model / Reference
362753 FDA UDI
Description
TUBE CPTHEP GC 16X125 8.0 MLBL RD/GN FDA UDI

Identifiers

Catalog Number
362753 FDA UDI
Primary DI / UDI-DI
30382903627531 FDA UDI
FDA Product Code
JCF FDA UDI
GMDN Term
Evacuated blood collection tube IVD, anticoagulant/separator/density solution FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.8500 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Evacuated blood collection tube IVD, anticoagulant/separator/density solution

BD Vacutainer® CPT™ Cell Preparation Tube with Sodium Heparin by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Evacuated blood collection tube IVD, anticoagulant/separator/density solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d7ed6c6-a0d6-4ec9-90ef-09458015de37 35 fields · synced Jun 8, 2026