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Tipcam

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
TIPCAM FDA UDI
Generic Name
Rigid video intracranial/spinal endoscope FDA UDI
Device Name
TIPCAM®1 S 3D, 30°, 4 mm FDA UDI
Model / Reference
28164BA3D FDA UDI
Description
TIPCAM®1 S 3D, 30°, 4 mm FDA UDI

Identifiers

Catalog Number
28164BA3D FDA UDI
Primary DI / UDI-DI
04048551396001 FDA UDI
FDA Product Code
GWG FDA UDI
GMDN Term
Rigid video intracranial/spinal endoscope 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 video intracranial/spinal endoscope

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

Similar devices

Also classified as Rigid video intracranial/spinal endoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8f3fa64b-9a5b-403a-9573-bdda9bd8b48b 35 fields · synced May 30, 2026