← Back to catalogue

LePinkky

FDA UDI

Class II (US FDA UDI)

by Casco Bay Molding

Identity

Trade Name
LePinkky FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name
100% Medical grade silicone menstrual cup FDA UDI
Model / Reference
Std FDA UDI
Description
100% Medical grade silicone menstrual cup FDA UDI

Identifiers

Primary DI / UDI-DI
00195893409013 FDA UDI
FDA Product Code
HHE FDA UDI
GMDN Term
Menstrual cup/disc, non-latex, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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 cup/disc, non-latex, reusable

LePinkky by Casco Bay Molding — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual cup/disc, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Casco Bay Molding

Sources (1)

  • FDA UDI 72c51efe-58fe-4fa8-90c9-8c8918b81edc 33 fields · synced Jun 8, 2026