Identity
- Trade Name
- Marina Medical FDA UDI
- Generic Name
- Nasal saw FDA UDI
- Device Name
- Preservation Rhinoplasty: Concave Radix Saw FDA UDI
- Model / Reference
- 200-504 FDA UDI
- Description
- Preservation Rhinoplasty: Concave Radix Saw FDA UDI
Identifiers
- Catalog Number
- 200-504 FDA UDI
- Primary DI / UDI-DI
- 00840306805486 FDA UDI
- FDA Product Code
- KBB FDA UDI
- GMDN Term
- Nasal saw FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Safe FDA UDI
Category: Nasal saw
Marina Medical by Marina Medical Instruments, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Marina Medical Instruments, Inc.
Sources (1)
- FDA UDI aa2f8e34-b31a-4b24-87c7-69dfc4b694e5 35 fields · synced May 30, 2026