← Back to catalogue

High Pressure DISS Hose For CO2

FDA UDI

Class II (US FDA UDI)

by Bracco Diagnostics Inc.

Identity

Trade Name
High Pressure DISS Hose For CO2 FDA UDI
Generic Name
Gastrointestinal endoscopic insufflator FDA UDI
Device Name
High Pressure DISS Hose FDA UDI
Model / Reference
710604 FDA UDI
Description
High Pressure DISS Hose FDA UDI

Identifiers

Catalog Number
710604 FDA UDI
Primary DI / UDI-DI
30815112020805 FDA UDI
FDA Product Code
FCX FDA UDI
GMDN Term
Gastrointestinal endoscopic insufflator 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Gastrointestinal endoscopic insufflator

High Pressure DISS Hose For CO2 by Bracco Diagnostics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrointestinal endoscopic insufflator.

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

Sources (1)

  • FDA UDI 500ec108-b3db-4779-8d06-cd80594d632b 35 fields · synced Jun 8, 2026