← Back to catalogue

Atellica CH Trf

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica CH Trf FDA UDI
Generic Name
Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Transferrin (Tnf) - Atellica CH - RGT - 880T FDA UDI
Model / Reference
11097613 FDA UDI
Description
Transferrin (Tnf) - Atellica CH - RGT - 880T FDA UDI

Identifiers

Catalog Number
11097613 FDA UDI
Primary DI / UDI-DI
00630414596297 FDA UDI
510(k) Number
K992662 FDA UDI
FDA Product Code
JNM FDA UDI
GMDN Term
Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5880 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: Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry

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

Similar devices

Also classified as Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry.

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 c59794e4-c9d5-4063-a774-77e2c0cbfb49 37 fields · synced May 29, 2026