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Atellica CH ALT

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica CH ALT FDA UDI
Generic Name
Alanine aminotransferase (ALT) IVD, kit, spectrophotometry FDA UDI
Device Name
Alanine Aminotransferase (ALT) Atellica CH - RGT 2550T FDA UDI
Model / Reference
11097605 FDA UDI
Description
Alanine Aminotransferase (ALT) Atellica CH - RGT 2550T FDA UDI

Identifiers

Catalog Number
11097605 FDA UDI
Primary DI / UDI-DI
00630414596365 FDA UDI
FDA Product Code
CKA FDA UDI
GMDN Term
Alanine aminotransferase (ALT) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1030 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alanine aminotransferase (ALT) IVD, kit, spectrophotometry

Atellica CH ALT by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alanine aminotransferase (ALT) IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6577a5f-3216-4927-b5ba-e61808f8b7ed 36 fields · synced May 30, 2026