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Natural Cycles

FDA UDI

Class II (US FDA UDI)

by Natural Cycles Nordic AB

Identity

Trade Name
Natural Cycles FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Test, Pregnancy, Hcg, Over The Counter FDA UDI
Model / Reference
15 FDA UDI
Description
Test, Pregnancy, Hcg, Over The Counter FDA UDI

Identifiers

Primary DI / UDI-DI
07350014630155 FDA UDI
510(k) Number
K043443 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

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 human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Natural Cycles by Natural Cycles Nordic AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical.

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 d21f2c05-eee3-42d7-8d72-f0c17d970dac 34 fields · synced May 31, 2026