← Back to catalogue

Unico Powerspin Bx

FDA UDI

by United Products & Instruments, Inc.

Identity

Trade Name
UNICO POWERSPIN BX FDA UDI
Generic Name
Microhaematocrit centrifuge IVD FDA UDI
Device Name
POWERSPIN™ BX CENTRIFUGE, VARIABLE SPEED 1,000-11,000 RPM, 8 PLACE AND 24PLACE MICROHEMATOCRIT ROTOR, 0-99 MIN DIGITAL TIMER, 110V FDA UDI
Model / Reference
C884 FDA UDI
Description
POWERSPIN™ BX CENTRIFUGE, VARIABLE SPEED 1,000-11,000 RPM, 8 PLACE AND 24PLACE MICROHEMATOCRIT ROTOR, 0-99 MIN DIGITAL TIMER, 110V FDA UDI

Identifiers

Catalog Number
C884 FDA UDI
Primary DI / UDI-DI
00816668020102 FDA UDI
GMDN Term
Microhaematocrit centrifuge IVD FDA UDI

Classification

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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microhaematocrit centrifuge IVD

Unico Powerspin Bx by United Products & Instruments, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microhaematocrit centrifuge 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

Sources (1)

  • FDA UDI 81a3b327-3d7d-4a9f-b6b1-90256e8ab942 35 fields · synced May 30, 2026