← Back to catalogue

Spotcheck

FDA UDI

Class II (US FDA UDI)

by Astoria-Pacific, Inc.

Identity

Trade Name
SPOTCHECK FDA UDI
Generic Name
Galactose-1-phosphate uridyl transferase IVD, control FDA UDI
Device Name
UT System Control, 10 x 50 mL FDA UDI
Model / Reference
80-4065P10K FDA UDI
Description
UT System Control, 10 x 50 mL FDA UDI

Identifiers

Catalog Number
80-4065P10K FDA UDI
Primary DI / UDI-DI
00725609000182 FDA UDI
510(k) Number
K970277 FDA UDI
FDA Product Code
KQP FDA UDI
GMDN Term
Galactose-1-phosphate uridyl transferase IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1315 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Galactose-1-phosphate uridyl transferase IVD, control

Spotcheck by Astoria-Pacific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Galactose-1-phosphate uridyl transferase IVD, control.

Cleared under the same submission

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 ede6337a-fe66-4ab5-b14b-2ed02be49768 35 fields · synced Jun 8, 2026