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Lithotripsy Telescope bridge w.7Ch. working channel

FDA UDI

Class II (US FDA UDI)

by mahe medical gmbh

Identity

Trade Name
Lithotripsy Telescope bridge w.7Ch. working channel FDA UDI
Generic Name
Footrest FDA UDI
Device Name
Lithotripsy Telescope bridge w.7Ch. working channel FDA UDI
Model / Reference
35.009.15QL FDA UDI
Description
Lithotripsy Telescope bridge w.7Ch. working channel FDA UDI

Identifiers

Catalog Number
35.009.15QL FDA UDI
Primary DI / UDI-DI
EMAH3500915QL0 FDA UDI
FDA Product Code
JFL FDA UDI
GMDN Term
Footrest 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: Footrest

Lithotripsy Telescope bridge w.7Ch. working channel by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Footrest.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
mahe medical gmbh

Sources (1)

  • FDA UDI 5150b1e8-3c53-4c0c-bde0-c28a340950b7 35 fields · synced Jun 8, 2026