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Silver Scope

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
SILVER SCOPE FDA UDI
Generic Name
Flexible video gastroscope, reusable FDA UDI
Device Name
Medium Gastroscope 7.8/2.8/1100 NTSC FDA UDI
Model / Reference
13823NKS FDA UDI
Description
Medium Gastroscope 7.8/2.8/1100 NTSC FDA UDI

Identifiers

Primary DI / UDI-DI
04048551390221 FDA UDI
FDA Product Code
FDS FDA UDI
GMDN Term
Flexible video gastroscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Flexible video gastroscope, reusable

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

Similar devices

Also classified as Flexible video gastroscope, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI c0079d94-eff1-4758-86f6-1c3deebbf92d 33 fields · synced Jun 8, 2026