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Atellica IM T3

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica IM T3 FDA UDI
Generic Name
Total triiodothyronine (TT3) IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
T3 Total (T3) Atellica IM - RGT 600T FDA UDI
Model / Reference
10995678 FDA UDI
Description
T3 Total (T3) Atellica IM - RGT 600T FDA UDI

Identifiers

Catalog Number
10995678 FDA UDI
Primary DI / UDI-DI
00630414599915 FDA UDI
510(k) Number
K041133 FDA UDI
FDA Product Code
CDP FDA UDI
GMDN Term
Total triiodothyronine (TT3) IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1710 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: Total triiodothyronine (TT3) IVD, kit, chemiluminescent immunoassay

Atellica IM T3 by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total triiodothyronine (TT3) IVD, kit, chemiluminescent immunoassay.

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 275173df-3298-435f-b411-09079f4d1a18 37 fields · synced Jun 8, 2026