Identity
- Trade Name
- Natrelle 410 Resterilizable Sizers FDA UDI
- Generic Name
- Invasive breast implant sizer, fixed, reusable FDA UDI
- Device Name
- NATRELLE 410 Rester Szr Sty MSZ-FM550 FDA UDI
- Model / Reference
- MSZFM550 FDA UDI
- Description
- NATRELLE 410 Rester Szr Sty MSZ-FM550 FDA UDI
Identifiers
- Catalog Number
- MSZFM550 FDA UDI
- Primary DI / UDI-DI
- 10888628004870 FDA UDI
- FDA Product Code
- MRD FDA UDI
- GMDN Term
- Invasive breast implant sizer, fixed, reusable FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dry Heat Sterilization FDA UDI
MR Safe FDA UDI
Natrelle 410 Resterilizable Sizers 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 3beefd59-de00-440a-9878-db359da04f40 37 fields · synced May 31, 2026