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Ch24 round silicone catheter

FDA UDI

Class I (US FDA UDI)

by Rand Spa

Identity

Trade Name
Ch24 round silicone catheter FDA UDI
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Model / Reference
001 FDA UDI

Identifiers

Catalog Number
R9900099 FDA UDI
Primary DI / UDI-DI
M640R99000990011 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage catheter 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

Yes

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

Dimensions & Sizes

Size
Length — 600 Millimeter FDA UDI
Catheter Gauge — 24 French FDA UDI

Category: Multi-purpose percutaneous abdominothoracic drainage catheter

Ch24 round silicone catheter by Rand Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose percutaneous abdominothoracic drainage catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rand Spa

Sources (1)

  • FDA UDI fde83105-138f-47d1-93c8-7c2c5b447bf1 35 fields · synced May 30, 2026