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Atellica IM TNIH

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica IM TNIH FDA UDI
Generic Name
Troponin I IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
High Sensitivity Troponin I (TnIH) Atellica IM Assay Kit 100T FDA UDI
Model / Reference
10997840 FDA UDI
Description
High Sensitivity Troponin I (TnIH) Atellica IM Assay Kit 100T FDA UDI

Identifiers

Catalog Number
10997840 FDA UDI
Primary DI / UDI-DI
00630414006703 FDA UDI
FDA Product Code
MMI FDA UDI
GMDN Term
Troponin I IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1215 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: Troponin I IVD, kit, chemiluminescent immunoassay

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

Similar devices

Also classified as Troponin I IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d675023c-26a6-4e5d-aa9e-b4c23e5a1a97 36 fields · synced May 30, 2026