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Metal Catheter

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
Metal Catheter FDA UDI
Generic Name
Ureteral catheter FDA UDI
Device Name
Metal Catheter Male for men 8 Fr., 29 cm FDA UDI
Model / Reference
320-720-080 FDA UDI
Description
Metal Catheter Male for men 8 Fr., 29 cm FDA UDI

Identifiers

Primary DI / UDI-DI
04049197264310 FDA UDI
FDA Product Code
GBZ FDA UDI
GMDN Term
Ureteral 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ureteral catheter

Metal Catheter by RZ-Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ureteral catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51155eae-59dc-4ffc-81a6-88e4159a10a6 33 fields · synced May 30, 2026