Identity
- Trade Name
- Dermaspan TM Tissue Expander FDA UDI
- Generic Name
- Skin-port tissue expander FDA UDI
- Device Name
- Dermaspan™ Low Pole Plus Tissue Expander Textured Surface w/ Lateral Extentions FDA UDI
- Model / Reference
- LPP13 FDA UDI
- Description
- Dermaspan™ Low Pole Plus Tissue Expander Textured Surface w/ Lateral Extentions FDA UDI
Identifiers
- Catalog Number
- LPP13 FDA UDI
- Primary DI / UDI-DI
- M746LPP130 FDA UDI
- FDA Product Code
- LCJ FDA UDI
- GMDN Term
- Skin-port tissue expander FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
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
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Width — 13 Centimeter FDA UDI
Dermaspan TM Tissue Expander by Specialty Surgical Products, Inc. — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Specialty Surgical Products, Inc.
Sources (1)
- FDA UDI ba13b84b-996f-44d2-afa8-886116a21983 37 fields · synced May 31, 2026