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b.pure

FDA UDI

Class II (US FDA UDI)

by Fourstar Group Inc.

Identity

Trade Name
b.pure FDA UDI
Generic Name
Menstrual pad, scented FDA UDI
Device Name
BPURE INFUSED OVRNGHT PADS 6CT FDA UDI
Model / Reference
64431638B FDA UDI
Description
BPURE INFUSED OVRNGHT PADS 6CT FDA UDI

Identifiers

Primary DI / UDI-DI
00049696889827 FDA UDI
FDA Product Code
HHL FDA UDI
GMDN Term
Menstrual pad, scented FDA UDI

Classification

Device Class
Class II 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Menstrual pad, scented

b.pure by Fourstar Group Inc. — Class II — 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

Manufacturer
Fourstar Group Inc.

Sources (1)

  • FDA UDI dab992d9-5479-481d-a81f-83764334f45e 33 fields · synced May 30, 2026