Identity
- Trade Name
- ONETRAC LXS FDA UDI
- Generic Name
- Surgical/emergency suction cannula, illuminating, single-use FDA UDI
- Device Name
- ONETRAC LXS single-use suction device with integrated cordless radial LED light source, Frazier, 8 Fr FDA UDI
- Model / Reference
- Frazier - 8 Fr FDA UDI
- Description
- ONETRAC LXS single-use suction device with integrated cordless radial LED light source, Frazier, 8 Fr FDA UDI
Identifiers
- Catalog Number
- C110310 FDA UDI
- Primary DI / UDI-DI
- 00850040140453 FDA UDI
- FDA Product Code
- JOL FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, illuminating, single-use 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
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
Yes
FDA UDI
Category: Surgical/emergency suction cannula, illuminating, single-use
Onetrac Lxs by Obp Surgical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical/emergency suction cannula, illuminating, single-use.
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- PhotonSaber F — Stryker Corp. · Class II
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
- Obp Surgical Corporation
Sources (1)
- FDA UDI 39207eb8-f41e-4ce5-91f7-46584c04b995 36 fields · synced May 31, 2026