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Pointe Scientific, Inc.

FDA UDI

Class II (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Scientific, Inc. FDA UDI
Generic Name
Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
U-TSH for the quantitative determination of the thyroid stimulating hormone (TSH) concentration in human serum. For in vitro diagnostic use only. 96 Tests. FDA UDI
Model / Reference
T1003-96 FDA UDI
Description
U-TSH for the quantitative determination of the thyroid stimulating hormone (TSH) concentration in human serum. For in vitro diagnostic use only. 96 Tests. FDA UDI

Identifiers

Catalog Number
T1003-96 FDA UDI
Primary DI / UDI-DI
00811727013187 FDA UDI
FDA Product Code
JLW FDA UDI
GMDN Term
Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1690 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

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

Category: Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA)

Pointe Scientific, Inc. by Pointe Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7b990588-e2ae-4c19-9b40-9614880562f4 36 fields · synced May 30, 2026