← Back to catalogue

Angel Blood Access Kits

FDA UDI

Class II (US FDA UDI)

by Nuo Therapeutics, Inc.

Identity

Trade Name
Angel Blood Access Kits FDA UDI
Generic Name
Phlebotomy kit FDA UDI
Device Name
Angel Blood Access Kits (NA) Single Unit (kit or Tray) with 966100258 Outer Box Label NA FDA UDI
Model / Reference
976000502 FDA UDI
Description
Angel Blood Access Kits (NA) Single Unit (kit or Tray) with 966100258 Outer Box Label NA FDA UDI

Identifiers

Primary DI / UDI-DI
00852714003033 FDA UDI
FDA Product Code
ORG FDA UDI
GMDN Term
Phlebotomy kit 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Phlebotomy kit

Angel Blood Access Kits by Nuo Therapeutics, Inc. — Class II — 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

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

Manufacturer

Sources (1)

  • FDA UDI 0f178c4a-b0a3-4359-b2ad-c4484a7c60c6 33 fields · synced Jun 8, 2026