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Atellica CH Amm

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica CH Amm FDA UDI
Generic Name
Ammonia IVD, kit, spectrophotometry FDA UDI
Device Name
Ammonia (Amm) Atellica CH – RGT 480T FDA UDI
Model / Reference
11097529 FDA UDI
Description
Ammonia (Amm) Atellica CH – RGT 480T FDA UDI

Identifiers

Catalog Number
11097529 FDA UDI
Primary DI / UDI-DI
00630414595832 FDA UDI
510(k) Number
K123320 FDA UDI
FDA Product Code
JIF FDA UDI
GMDN Term
Ammonia IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1065 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ammonia IVD, kit, spectrophotometry

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

Similar devices

Also classified as Ammonia IVD, kit, spectrophotometry.

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 1d5bc684-c728-462e-9f78-b186f070f3a4 37 fields · synced May 30, 2026