Identity
- Trade Name
- Poise FDA UDI
- Generic Name
- Urinary-incontinence vaginal insert, single-use FDA UDI
- Device Name
- POISE IMPRESSA BLADDER SUPPORT DEVICE FDA UDI
- Model / Reference
- Pessary FDA UDI
- Description
- POISE IMPRESSA BLADDER SUPPORT DEVICE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00036000411164 FDA UDI
- FDA Product Code
- HHW FDA UDI
- GMDN Term
- Urinary-incontinence vaginal insert, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.3575 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Width — 40 Millimeter FDA UDIWidth — 50 Millimeter FDA UDI
Poise by Kimberly-Clark Global Sales, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Kimberly-Clark Global Sales, Inc.
Sources (1)
- FDA UDI 55e1b0c9-1d51-4433-a1a0-28a0f7e2e46f 36 fields · synced May 31, 2026