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Jeffery

FDA UDI

Class I (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Jeffery FDA UDI
Generic Name
Non-vascular catheter introduction set FDA UDI
Device Name
Jeffery Wire Guide Exchange Set With Nitinol Wire Guide FDA UDI
Model / Reference
G08602 FDA UDI
Description
Jeffery Wire Guide Exchange Set With Nitinol Wire Guide FDA UDI

Identifiers

Catalog Number
JWGE-104-NT FDA UDI
Primary DI / UDI-DI
00827002086029 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Non-vascular catheter introduction set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Non-vascular catheter introduction set

Jeffery by Cook Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-vascular catheter introduction set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI a6b06134-2a28-4000-9f33-662e1a18ea6d 36 fields · synced Jun 8, 2026