Identity
- Trade Name
- Restore FDA UDI
- Generic Name
- Secretion/excreta skin cleanser FDA UDI
- Device Name
- Dermal Wound Cleanser FDA UDI
- Model / Reference
- 529975 FDA UDI
- Description
- Dermal Wound Cleanser FDA UDI
Identifiers
- Catalog Number
- 529975 FDA UDI
- Primary DI / UDI-DI
- 00610075059775 FDA UDI
- FDA Product Code
- FRO FDA UDI
- GMDN Term
- Secretion/excreta skin cleanser FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Secretion/excreta skin cleanser
Restore by Hollister Incorporated — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Hollister Incorporated
Sources (1)
- FDA UDI 08dd7279-5b8a-4363-8bdb-a5943c42bb88 35 fields · synced Jun 9, 2026