← Back to catalogue

Endocameleon

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
ENDOCAMELEON FDA UDI
Generic Name
Rigid optical intracranial/spinal endoscope, reusable FDA UDI
Device Name
ENDOCAMELEON® HOPKINS® Telescope FDA UDI
Model / Reference
28132AE FDA UDI
Description
ENDOCAMELEON® HOPKINS® Telescope FDA UDI

Identifiers

Primary DI / UDI-DI
04048551326572 FDA UDI
FDA Product Code
GWG FDA UDI
GMDN Term
Rigid optical intracranial/spinal endoscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1480 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical intracranial/spinal endoscope, reusable

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

Similar devices

Also classified as Rigid optical intracranial/spinal endoscope, reusable.

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
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI a03044df-d2a9-4918-a536-75d1922d8d9f 33 fields · synced May 30, 2026