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Rapid Response

FDA UDI

Class I (US FDA UDI)

by BTNX Inc

Identity

Trade Name
Rapid Response FDA UDI
Generic Name
Follicle stimulating hormone (FSH) IVD, kit, immunochromatographic test (ICT), rapid, professional/self-test FDA UDI
Device Name
Rapid Response FSH Menopause Test Cassette (Urine) - 25 tests/ kit for the qualitative detection of Follicle-stimulating hormone in urine. FDA UDI
Model / Reference
FSH-1C25 FDA UDI
Description
Rapid Response FSH Menopause Test Cassette (Urine) - 25 tests/ kit for the qualitative detection of Follicle-stimulating hormone in urine. FDA UDI

Identifiers

Primary DI / UDI-DI
10722066005337 FDA UDI
FDA Product Code
NGA FDA UDI
GMDN Term
Follicle stimulating hormone (FSH) IVD, kit, immunochromatographic test (ICT), rapid, professional/self-test FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1300 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Follicle stimulating hormone (FSH) IVD, kit, immunochromatographic test (ICT), rapid, professional/self-test

Rapid Response by BTNX Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Follicle stimulating hormone (FSH) IVD, kit, immunochromatographic test (ICT), rapid, professional/self-test.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BTNX Inc

Sources (1)

  • FDA UDI 71028fe4-dd36-4003-8159-c2fda98ac904 33 fields · synced Jun 8, 2026