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Natural Cycles Application

FDA UDI

Class II (US FDA UDI)

by Natural Cycles Nordic AB

Identity

Trade Name
Natural Cycles Application FDA UDI
Generic Name
Self-care monitoring/reporting software FDA UDI
Model / Reference
V5.4.0 FDA UDI

Identifiers

Primary DI / UDI-DI
07350014630339 FDA UDI
FDA Product Code
PYT FDA UDI
GMDN Term
Self-care monitoring/reporting software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5370 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

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: Self-care monitoring/reporting software

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

Similar devices

Also classified as Self-care monitoring/reporting software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e53f93a-6b66-4ca3-9ee2-e784bed2cb11 32 fields · synced May 29, 2026