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Fogarty Everclip

FDA UDI

Class II (US FDA UDI)

by Edwards Lifesciences LLC

Identity

Trade Name
FOGARTY EVERCLIP FDA UDI
Generic Name
Vascular clamp, single-use FDA UDI
Device Name
EVERCLIP 6MM SPRING CLIP LATEX FREE 10/CS FDA UDI
Model / Reference
EVERCLIP6 FDA UDI
Description
EVERCLIP 6MM SPRING CLIP LATEX FREE 10/CS FDA UDI

Identifiers

Catalog Number
EVERCLIP6 FDA UDI
Primary DI / UDI-DI
00690103160406 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Vascular clamp, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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: Vascular clamp, single-use

Fogarty Everclip by Edwards Lifesciences LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular clamp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Edwards Lifesciences LLC

Sources (1)

  • FDA UDI e4d4fb32-b91d-4dc9-b3af-0be43848c174 37 fields · synced Jun 6, 2026