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Shuttle Select Slip-Cath

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Shuttle Select Slip-Cath FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
Shuttle, Select Slip-Cath, 5Fr Shuttle, System Compatible FDA UDI
Model / Reference
G36360 FDA UDI
Description
Shuttle, Select Slip-Cath, 5Fr Shuttle, System Compatible FDA UDI

Identifiers

Catalog Number
SCBR5.5-35-125-P-NS-SIM2-SHTL FDA UDI
Primary DI / UDI-DI
00827002363601 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Angiographic catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Angiographic catheter, single-use

Shuttle Select Slip-Cath by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI ee85f730-df61-48b4-8d3d-69be3899d25e 36 fields · synced Jun 8, 2026