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Reprocessed Apollo RF Aspirating Ablator 50, Multi-Port
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Reprocessed Apollo RF Aspirating Ablator 50, Multi-Port FDA UDI
- Generic Name
- Arthroscopic shaver system blade, reprocessed FDA UDI
- Device Name
- Apollo RF MP50, Aspirating Ablator 50°, Multi-Port FDA UDI
- Model / Reference
- AR-9815 FDA UDI
- Description
- Apollo RF MP50, Aspirating Ablator 50°, Multi-Port FDA UDI
Identifiers
- Primary DI / UDI-DI
- B390AR98151 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Arthroscopic shaver system blade, reprocessed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Reprocessed Apollo RF Aspirating Ablator 50, Multi-Port by Suretek Medical — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Suretek Medical
Sources (1)
- FDA UDI f8aa54c1-a567-479c-9f46-f711e6ec7db7 34 fields · synced Jun 6, 2026