Identity
- Trade Name
- Curity FDA UDI
- Generic Name
- Menstrual pad, unscented FDA UDI
- Device Name
- Peri-Pad,Moderate FDA UDI
- Model / Reference
- 1380A FDA UDI
- Description
- Peri-Pad,Moderate FDA UDI
Identifiers
- Catalog Number
- 1380A FDA UDI
- Primary DI / UDI-DI
- 20884521157665 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
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
Dimensions & Sizes
- Size
- Length — 10 Inch FDA UDIWidth — 3.75 Inch FDA UDI
Category: Menstrual pad, unscented
Curity by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Cardinalhealth
Sources (1)
- FDA UDI 12a33786-4a3c-48df-9cca-ae90f7279871 37 fields · synced May 30, 2026