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ClosureFast™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
ClosureFast™ FDA UDI
Generic Name
Peripheral vascular electrocautery catheter, single-use FDA UDI
Device Name
Catheter CF7-7-60 Closure Fast V04 FDA UDI
Model / Reference
CF7-7-60 FDA UDI
Description
Catheter CF7-7-60 Closure Fast V04 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000022273 FDA UDI
510(k) Number
K061373 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Peripheral vascular electrocautery catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.3 Millimeter FDA UDI
Catheter Gauge — 7.0 French FDA UDI

Category: Peripheral vascular electrocautery catheter, single-use

ClosureFast™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular electrocautery catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 32d20901-ed10-4952-8bce-11300e7cce10 37 fields · synced May 30, 2026