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Angel Whole Blood Processing System Machine - EU - Reworked

FDA UDI

Class II (US FDA UDI)

by Nuo Therapeutics, Inc.

Identity

Trade Name
Angel Whole Blood Processing System Machine - EU - Reworked FDA UDI
Generic Name
Apheresis system FDA UDI
Device Name
Angel Whole Blood Processing System Machine - EU - Reworked with 020162 EU Case Label for Refurbished Machines FDA UDI
Model / Reference
976000901 FDA UDI
Description
Angel Whole Blood Processing System Machine - EU - Reworked with 020162 EU Case Label for Refurbished Machines FDA UDI

Identifiers

Primary DI / UDI-DI
00852714003088 FDA UDI
FDA Product Code
ORG FDA UDI
GMDN Term
Apheresis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9245 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

No

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: Apheresis system

Angel Whole Blood Processing System Machine - EU - Reworked by Nuo Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Apheresis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4bcb5e6b-f368-478f-ba4b-282a7cb6d0dd 33 fields · synced May 30, 2026