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Spotcheck

FDA UDI

Class I (US FDA UDI)

by Astoria-Pacific, Inc.

Identity

Trade Name
SPOTCHECK FDA UDI
Generic Name
Multichannel clinical chemistry analyser IVD, laboratory FDA UDI
Device Name
Uridyltransferase Blank Cartridge FDA UDI
Model / Reference
307-A980-00B FDA UDI
Description
Uridyltransferase Blank Cartridge FDA UDI

Identifiers

Catalog Number
307-A980-00B FDA UDI
Primary DI / UDI-DI
00725609000380 FDA UDI
510(k) Number
K101392 FDA UDI
FDA Product Code
JJC FDA UDI
GMDN Term
Multichannel clinical chemistry analyser IVD, laboratory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2150 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

No

FDA UDI

Category: Multichannel clinical chemistry analyser IVD, laboratory

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

Similar devices

Also classified as Multichannel clinical chemistry analyser IVD, laboratory.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 14e769da-4fe1-4c5c-8b3b-3719341455d9 35 fields · synced Jun 8, 2026