← Back to catalogue

Cysto.-Urethro.-sheath, compl., 19Ch.

FDA UDI

Class II (US FDA UDI)

by mahe medical gmbh

Identity

Trade Name
Cysto.-Urethro.-sheath,compl.,19Ch. FDA UDI
Generic Name
Rigid endoscope working guide FDA UDI
Device Name
Cysto.-Urethro.-sheath,compl.,19Ch. FDA UDI
Model / Reference
35.007.05 FDA UDI
Description
Cysto.-Urethro.-sheath,compl.,19Ch. FDA UDI

Identifiers

Catalog Number
35.007.05 FDA UDI
Primary DI / UDI-DI
EMAH35007050 FDA UDI
FDA Product Code
JFL FDA UDI
GMDN Term
Rigid endoscope working guide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1160 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

Category: Rigid endoscope working guide

Cysto.-Urethro.-sheath, compl., 19Ch. by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscope working guide.

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
mahe medical gmbh

Sources (1)

  • FDA UDI 9449dfdc-8064-4e49-9a38-3e59d3eab83e 35 fields · synced May 30, 2026