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iProven

FDA UDI

Class I (US FDA UDI)

by Sevenground Trading B.V.

Identity

Trade Name
iProven FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI
Device Name
FK-127A contains 50 ovulation test and 20 pregnancy tests. FDA UDI
Model / Reference
FK-127-CO FDA UDI
Description
FK-127A contains 50 ovulation test and 20 pregnancy tests. FDA UDI

Identifiers

Primary DI / UDI-DI
08719699634633 FDA UDI
FDA Product Code
CEP FDA UDI
LCX FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1485 FDA UDI
862.1155 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical

iProven by Sevenground Trading B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b26b50b1-daa1-4ac6-be1f-194bd0c372e7 34 fields · synced May 30, 2026