← Back to catalogue

Atellica CH AAT

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica CH AAT FDA UDI
Generic Name
Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Alpha-1-Acid-Antitrypsin (AAT) Atellica CH RGT 360T FDA UDI
Model / Reference
11097628 FDA UDI
Description
Alpha-1-Acid-Antitrypsin (AAT) Atellica CH RGT 360T FDA UDI

Identifiers

Catalog Number
11097628 FDA UDI
Primary DI / UDI-DI
00630414596228 FDA UDI
510(k) Number
K031857 FDA UDI
FDA Product Code
DEM FDA UDI
GMDN Term
Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5130 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: Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry

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

Similar devices

Also classified as Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry.

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 953e006a-8777-499a-9745-f6b3de000407 37 fields · synced May 30, 2026