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Seventh Generation

FDA UDI

Class I (US FDA UDI)

by Seventh Generation

Identity

Trade Name
Seventh Generation FDA UDI
Generic Name
Menstrual pad, unscented FDA UDI
Device Name
100 ct Pantiliners FDA UDI
Model / Reference
Liner FDA UDI
Description
100 ct Pantiliners FDA UDI

Identifiers

Primary DI / UDI-DI
00732913446834 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Menstrual pad, unscented

Seventh Generation by Seventh Generation — 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
Seventh Generation

Sources (1)

  • FDA UDI 93b3ff88-fd66-42f6-992f-75246ba5da76 33 fields · synced Jun 6, 2026