Identity
- Trade Name
- Poise FDA UDI
- Generic Name
- Menstrual pad, unscented FDA UDI
- Device Name
- Sample pack contains one of each: 1) One by Poise Extra Coverage Liner (53451-00),2) One by Poise Heavy Pad (53452-00), 3) One by Poise Reg Pad (53453-00) FDA UDI
- Model / Reference
- Pad FDA UDI
- Description
- Sample pack contains one of each: 1) One by Poise Extra Coverage Liner (53451-00),2) One by Poise Heavy Pad (53452-00), 3) One by Poise Reg Pad (53453-00) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00036000670035 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
Yes
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 pad, unscented
Poise by Kimberly-Clark Global Sales, Inc. — 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
- Kimberly-Clark Global Sales, Inc.
Sources (1)
- FDA UDI d6ab84e2-2fee-473d-80db-ebd32be3a738 34 fields · synced May 30, 2026