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Carefree

FDA UDI

Class I (US FDA UDI)

by Edgewell Personal Care Brands, Llc

Identity

Trade Name
Carefree FDA UDI
Generic Name
Menstrual pad, scented FDA UDI
Device Name
CF BODYSHAPE THIN QW OC 22 FDA UDI
Model / Reference
06991 FDA UDI
Description
CF BODYSHAPE THIN QW OC 22 FDA UDI

Identifiers

Primary DI / UDI-DI
00078300069911 FDA UDI
FDA Product Code
NRC FDA UDI
GMDN Term
Menstrual pad, scented FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5425 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Menstrual pad, scented

Carefree by Edgewell Personal Care Brands, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual pad, scented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 503a4e2c-29de-409b-9bad-312ffa41ac5f 33 fields · synced Jun 6, 2026