← Back to catalogue

Ciaglia Blue Rhino G2

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Ciaglia Blue Rhino G2 FDA UDI
Generic Name
Tracheostomy kit, single-use FDA UDI
Device Name
Ciaglia Blue Rhino G2 Advanced Percutaneous Tracheostomy Introducer Tray FDA UDI
Model / Reference
G53176 FDA UDI
Description
Ciaglia Blue Rhino G2 Advanced Percutaneous Tracheostomy Introducer Tray FDA UDI

Identifiers

Catalog Number
C-PTISY-100-FLEX-HC-G FDA UDI
Primary DI / UDI-DI
00827002531765 FDA UDI
FDA Product Code
JOH FDA UDI
GMDN Term
Tracheostomy kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

Yes

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: Tracheostomy kit, single-use

Ciaglia Blue Rhino G2 by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy kit, 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 b006431f-98e4-457e-8508-0f92a800569e 36 fields · synced Jun 8, 2026