Identity
- Trade Name
- Marina Medical FDA UDI
- Generic Name
- Open-surgery dissector FDA UDI
- Device Name
- Rz5: Glabellar, Superior Orbital Rim and Arcus Marginalis Dissector FDA UDI
- Model / Reference
- 150-106 FDA UDI
- Description
- Rz5: Glabellar, Superior Orbital Rim and Arcus Marginalis Dissector FDA UDI
Identifiers
- Catalog Number
- 150-106 FDA UDI
- Primary DI / UDI-DI
- 00840306803826 FDA UDI
- FDA Product Code
- GDI FDA UDI
- GMDN Term
- Open-surgery dissector FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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: Open-surgery dissector
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 0e60ce5b-22e1-4da3-a149-4bd3e2258765 35 fields · synced May 29, 2026