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Breeze

FDA UDI

Class I (US FDA UDI)

by Dolgencorp, Llc

Identity

Trade Name
BREEZE FDA UDI
Generic Name
Menstrual pad, unscented FDA UDI
Device Name
ULTRA THIN PAD WING OVERNIGHT UNSCENTED 28 CT FDA UDI
Model / Reference
34201701 FDA UDI
Description
ULTRA THIN PAD WING OVERNIGHT UNSCENTED 28 CT FDA UDI

Identifiers

Primary DI / UDI-DI
00090891949700 FDA UDI
FDA Product Code
HHD FDA UDI
GMDN Term
Menstrual pad, unscented FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5435 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Menstrual pad, unscented

Breeze by Dolgencorp, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual pad, unscented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dolgencorp, Llc

Sources (1)

  • FDA UDI eacc9d2c-78eb-49a6-be4f-d100e6442485 33 fields · synced May 31, 2026