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S-Pilot

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
S-PILOT FDA UDI
Generic Name
Endoscope air/water valve, reusable FDA UDI
Device Name
S-PILOT FDA UDI
Model / Reference
UP501 FDA UDI
Description
S-PILOT FDA UDI

Identifiers

Catalog Number
UP501 FDA UDI
Primary DI / UDI-DI
04048551354155 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Endoscope air/water valve, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope air/water valve, reusable

S-Pilot by Karl Storz GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope air/water valve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d58b613a-ef19-4a3d-bcca-975168c8a7ee 35 fields · synced Jun 8, 2026