Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
- Device Name
- SUCTION TUBE, INTERCHANGEABLE Ø 5 MM W-L 330 MM FOR HANDLE T.0510.01 FDA UDI
- Model / Reference
- T.0510.03 FDA UDI
- Description
- SUCTION TUBE, INTERCHANGEABLE Ø 5 MM W-L 330 MM FOR HANDLE T.0510.01 FDA UDI
Identifiers
- Catalog Number
- T.0510.03 FDA UDI
- Primary DI / UDI-DI
- 04049047097679 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
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
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
Category: Surgical irrigation/aspiration cannula, non-illuminating, reusable
Gimmi by Gimmi GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical irrigation/aspiration cannula, non-illuminating, reusable.
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- Modulap — ATC TECHNOLOGIES INC. · Class II
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Gimmi GmbH
Sources (1)
- FDA UDI b09ac7e0-ace6-4cce-ab02-fb2ab2d02839 35 fields · synced May 30, 2026