Identity
- Trade Name
- GEN2 FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
- Device Name
- HOWINGTON SUCTION,8FR Atraumatic Tip W/NO Side Holes 1'' Bend 5'' Distal Tip, 6'' OL FDA UDI
- Model / Reference
- G2NHX29085 FDA UDI
- Description
- HOWINGTON SUCTION,8FR Atraumatic Tip W/NO Side Holes 1'' Bend 5'' Distal Tip, 6'' OL FDA UDI
Identifiers
- Catalog Number
- G2NHX29085 FDA UDI
- Primary DI / UDI-DI
- 00840343726904 FDA UDI
- FDA Product Code
- JOL FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
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
Dimensions & Sizes
- Size
- Catheter Gauge — 8 French FDA UDILength — 6 Inch FDA UDI
Category: Surgical/emergency suction cannula, non-illuminating, reusable
Gen2 by Surgix Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.
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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
- Surgix Medical Llc
Sources (1)
- FDA UDI bb937226-64e2-41b0-abcd-eb79cbf8cc84 36 fields · synced Jun 1, 2026