Identity
- Trade Name
- Vital Vue FDA UDI
- Generic Name
- Surgical/emergency suction cannula, illuminating, single-use FDA UDI
- Device Name
- Orthopedic Tip Instrument FDA UDI
- Model / Reference
- 8886828306 FDA UDI
- Description
- Orthopedic Tip Instrument FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521176119 FDA UDI
- 510(k) Number
- K883201 FDA UDI
- FDA Product Code
- HBI FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, illuminating, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4580 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical/emergency suction cannula, illuminating, single-use
Vital Vue by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical/emergency suction cannula, illuminating, single-use.
- Eigr™ Saber Waveguide — INVUITY, INC. · Class II
- Spetzler™ Lighted Suction Tube, 7 French, 140mm long — KATALYST SURGICAL, LLC · Class II
- Spetzler Lighted Suction Tube, 7 French 160mm, Storz Connector — KATALYST SURGICAL, LLC · Class II
- PhotonSaber Y — Stryker Corp. · Class II
- Spetzler™ Lighted Suction Tube, 5 French, 120mm long — KATALYST SURGICAL, LLC · Class II
- Spetzler Lighted Suction Tube, 5 French, 120mm, Storz Connector — KATALYST SURGICAL, LLC · Class II
- PhotonSaber F — Stryker Corp. · Class II
- Spetzler™ Lighted Suction Tube, 3 French, 120mm long — KATALYST SURGICAL, LLC · Class II
Cleared under the same submission
K883201 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Covidien LP
Sources (1)
- FDA UDI d6ae4708-9ef1-4ff7-9a48-6448aac79cec 35 fields · synced May 30, 2026