Identity
- Trade Name
- Flex FDA UDI
- Generic Name
- Menstrual cup/disc, non-latex, single-use FDA UDI
- Device Name
- Flex Disc 2 ct. FDA UDI
- Model / Reference
- 10268 FDA UDI
- Description
- Flex Disc 2 ct. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850037498420 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
Yes
FDA UDI
Category: Menstrual cup/disc, non-latex, single-use
Flex 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.
- Flex — The Flex Company · Class II
- Flex — The Flex Company · Class II
- Flex — The Flex Company · Class II
- Softdisc — The Flex Company · Class II
- Softcup — The Flex Company · Class II
- Flex — The Flex Company · Class II
- Flex — The Flex Company · Class II
- Flex — The Flex Company · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- The Flex Company
Sources (1)
- FDA UDI 7f19adae-d479-461d-9296-a06640fc23c8 34 fields · synced May 30, 2026