Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Surgical irrigation/aspiration cannula, illuminating, reusable FDA UDI
- Device Name
- Suction Tube, 90 °, angled downwards, 8 1/2", (215 mm), 5FR, non-sterile, reusable FDA UDI
- Model / Reference
- MF106R FDA UDI
- Description
- Suction Tube, 90 °, angled downwards, 8 1/2", (215 mm), 5FR, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- MF106R FDA UDI
- Primary DI / UDI-DI
- 04046964676451 FDA UDI
- FDA Product Code
- JOL FDA UDI
- GMDN Term
- Surgical irrigation/aspiration cannula, illuminating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Aesculap by Aesculap, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI 347c9c60-eefa-4cc3-b3f6-b0dc67495fa0 36 fields · synced Jun 1, 2026