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Flex Cup and Flex Disc

FDA UDI

Class II (US FDA UDI)

by The Flex Company

Identity

Trade Name
Flex Cup and Flex Disc FDA UDI
Generic Name
Menstrual cup/disc, non-latex, single-use FDA UDI
Device Name
Flex Cup Size 1 and 2 Flex Discs (English only) FDA UDI
Model / Reference
Flex Discovery Kit Slim Fit FDA UDI
Description
Flex Cup Size 1 and 2 Flex Discs (English only) FDA UDI

Identifiers

Primary DI / UDI-DI
00851906007262 FDA UDI
FDA Product Code
HHE FDA UDI
GMDN Term
Menstrual cup/disc, non-latex, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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, single-use

Flex Cup and Flex Disc by The Flex Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
The Flex Company

Sources (1)

  • FDA UDI 18c95f68-76c9-4ffe-a675-df967af63fb6 34 fields · synced May 31, 2026