Identity
- Trade Name
- Natrelle® Style 133 Tissue Expanders FDA UDI
- Generic Name
- Skin-port tissue expander FDA UDI
- Device Name
- NATRELLE 133FX-11, 350 cc FDA UDI
- Model / Reference
- 133FX-11 FDA UDI
- Description
- NATRELLE 133FX-11, 350 cc FDA UDI
Identifiers
- Catalog Number
- 133FX-11 FDA UDI
- Primary DI / UDI-DI
- 10888628003989 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Natrelle® Style 133 Tissue Expanders by Allergan — 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
- Allergan
Sources (1)
- FDA UDI e916dc00-0050-4254-a8fa-5570a0563e50 37 fields · synced Jun 1, 2026