Identity
- Trade Name
- GAS TUBE FDA UDI
- Generic Name
- Endoscopic insufflation tubing set, reusable FDA UDI
- Device Name
- MA-238 GAS CONNECTING TUBE F/ CF-MB2/LB2 FDA UDI
- Model / Reference
- MA-238 FDA UDI
- Description
- MA-238 GAS CONNECTING TUBE F/ CF-MB2/LB2 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04953170064517 FDA UDI
- FDA Product Code
- FBN FDA UDI
- GMDN Term
- Endoscopic insufflation tubing set, 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
Yes
FDA UDI
Category: Endoscopic insufflation tubing set, reusable
Gas Tube by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic insufflation tubing set, reusable.
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- Hydra — Boston Scientific · Class II
- Protego Hybrid Tubing — GA Health Company Limited · Class II
- andorate® CO2 Source Tubing Adapter — GA Health Company Limited · Class I
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
- Olympus Medical Systems Corporation
Sources (1)
- FDA UDI 0fc38da8-d63b-47fb-bc66-96f66a72df50 34 fields · synced Jun 8, 2026