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Rite Aid Pharmacy

FDA UDI

Class I (US FDA UDI)

by Spd Swiss Precision Diagnostics Gmbh

Identity

Trade Name
Rite Aid Pharmacy FDA UDI
Generic Name
Natural conception assistance kit FDA UDI
Device Name
WWOT Rite Aid OVS FDA UDI
Model / Reference
Family Planning Ovulation Predictor One Step FDA UDI
Description
WWOT Rite Aid OVS FDA UDI

Identifiers

Primary DI / UDI-DI
00011822337373 FDA UDI
FDA Product Code
CEP FDA UDI
GMDN Term
Natural conception assistance kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1485 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Rite Aid Pharmacy by Spd Swiss Precision Diagnostics Gmbh — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7f10cea-6c93-429b-ba49-02bfe2091f94 36 fields · synced Jun 8, 2026