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T3 Uptake 125I RIA Kit

FDA UDI

Class II (US FDA UDI)

by Mp Biomedicals, Llc

Identity

Trade Name
T3 Uptake 125I RIA Kit FDA UDI
Generic Name
Reverse triiodothyronine (reverse T3) IVD, kit, radioimmunoassay FDA UDI
Device Name
Radioimmunoassay for the quantitative determination of the percentage of triiodothyronine (T3) Uptake in serum. FDA UDI
Model / Reference
06B237116 FDA UDI
Description
Radioimmunoassay for the quantitative determination of the percentage of triiodothyronine (T3) Uptake in serum. FDA UDI

Identifiers

Catalog Number
06B237116 FDA UDI
Primary DI / UDI-DI
00817830022429 FDA UDI
FDA Product Code
KHQ FDA UDI
GMDN Term
Reverse triiodothyronine (reverse T3) IVD, kit, radioimmunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1715 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Dimensions & Sizes

Size
Length — 28 Centimeter FDA UDI

Category: Reverse triiodothyronine (reverse T3) IVD, kit, radioimmunoassay

T3 Uptake 125I RIA Kit by Mp Biomedicals, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse triiodothyronine (reverse T3) IVD, kit, radioimmunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mp Biomedicals, Llc

Sources (1)

  • FDA UDI 4de80327-f78f-4d65-b65d-b0816c857f2b 37 fields · synced Jun 7, 2026