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Coil Expander

FDA UDI

Class I (US FDA UDI)

by Cook Vandergrift Inc.

Identity

Trade Name
Coil Expander FDA UDI
Generic Name
Pacing/defibrillation lead extraction expander FDA UDI
Device Name
Coil Expander FDA UDI
Model / Reference
G20005 FDA UDI
Description
Coil Expander FDA UDI

Identifiers

Catalog Number
LR-CEX001 FDA UDI
Primary DI / UDI-DI
00827002200050 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Pacing/defibrillation lead extraction expander FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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: Pacing/defibrillation lead extraction expander

Coil Expander by Cook Vandergrift Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Vandergrift Inc.

Sources (1)

  • FDA UDI dc91895d-ec85-41d8-8a2d-3274d8b8128e 36 fields · synced Jun 1, 2026