← Back to catalogue

Tracer Metro

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Tracer Metro FDA UDI
Generic Name
Gastro-urological guidewire, single-use FDA UDI
Device Name
Tracer Metro Direct Wire Guide FDA UDI
Model / Reference
G55137 FDA UDI
Description
Tracer Metro Direct Wire Guide FDA UDI

Identifiers

Catalog Number
METII-35-480-A-J FDA UDI
Primary DI / UDI-DI
00827002551374 FDA UDI
FDA Product Code
OCY FDA UDI
GMDN Term
Gastro-urological guidewire, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Gastro-urological guidewire, single-use

Tracer Metro by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological guidewire, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI ca2f613e-5246-4e0c-968b-cc27d4bbe426 36 fields · synced Jun 8, 2026