Identity
- Trade Name
- ClosureFast FDA UDI
- Generic Name
- Irrigation catheter, single-lumen FDA UDI
- Device Name
- Tumescent Pump Tubing Set,4 m FDA UDI
- Model / Reference
- TTUB-4 FDA UDI
- Description
- Tumescent Pump Tubing Set,4 m FDA UDI
Identifiers
- Catalog Number
- TTUB-4 FDA UDI
- Primary DI / UDI-DI
- 10884521140448 FDA UDI
- 510(k) Number
- K071588 FDA UDI
- FDA Product Code
- FRN FDA UDI
- GMDN Term
- Irrigation catheter, single-lumen FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 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
Dimensions & Sizes
- Size
- Length — 4 Meter FDA UDI
Category: Irrigation catheter, single-lumen
ClosureFast by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Irrigation catheter, single-lumen.
- Halyard — Avanos Medical, Inc. · Class II
- MD Resource — Medical Device Resource Corp. · Class I
- Halyard — Avanos Medical, Inc. · Class II
- Hobbs Aspiration Catheter — HOBBS MEDICAL, INC. · Class II
- Halyard — Avanos Medical, Inc. · Class II
- Halyard — Avanos Medical, Inc. · Class II
- Halyard — Avanos Medical, Inc. · Class II
- MD Resource — Medical Device Resource Corp. · Class I
Cleared under the same submission
K071588 also covers:
- ClosureFast — Covidien LP
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 — Nouvag AG
- Dispenser DP 30 LipoPlus — Nouvag AG
- Dispenser DP 30 LipoPlus — Nouvag AG
- Dispenser DP 30 LipoPlus — Nouvag AG
- Foot control On/Off — Nouvag AG
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 58724f11-5b53-4e1d-97fd-1038c64c1798 38 fields · synced May 30, 2026