← Back to catalogue

Platelet Aggregometer Profiler

FDA UDI

Class II (US FDA UDI)

by Bio/Data Corp.

Identity

Trade Name
Platelet Aggregometer Profiler FDA UDI
Generic Name
Platelet aggregation analyser IVD FDA UDI
Device Name
Platelet Aggregometer Profiler Model PAP-8E FDA UDI
Model / Reference
PAP8E FDA UDI
Description
Platelet Aggregometer Profiler Model PAP-8E FDA UDI

Identifiers

Catalog Number
106075 FDA UDI
Primary DI / UDI-DI
G0561060751 FDA UDI
FDA Product Code
JBX FDA UDI
GMDN Term
Platelet aggregation analyser IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Platelet aggregation analyser IVD

Platelet Aggregometer Profiler by Bio/Data Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Platelet aggregation analyser IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bio/Data Corp.

Sources (1)

  • FDA UDI 02de46d8-e826-4cf4-a657-4d1f0c4a3be3 34 fields · synced May 30, 2026