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ClosureFast

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
ClosureFast FDA UDI
Generic Name
Laboratory liquid dispenser, electronic FDA UDI
Device Name
Tumescent Pump Foot Pedal,On/Off Control FDA UDI
Model / Reference
TPED-T FDA UDI
Description
Tumescent Pump Foot Pedal,On/Off Control FDA UDI

Identifiers

Primary DI / UDI-DI
10884521140424 FDA UDI
510(k) Number
K071588 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Laboratory liquid dispenser, electronic 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laboratory liquid dispenser, electronic

ClosureFast by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory liquid dispenser, electronic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 77e61d93-cc74-4c50-b299-cc3c84ca66c7 35 fields · synced May 30, 2026