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Hopkins

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
HOPKINS FDA UDI
Generic Name
Rigid optical intracranial/spinal endoscope, reusable FDA UDI
Device Name
HOPKINS® Telescope 30°, 2.9 mm, 30 cm FDA UDI
Model / Reference
28160BA FDA UDI
Description
HOPKINS® Telescope 30°, 2.9 mm, 30 cm FDA UDI

Identifiers

Primary DI / UDI-DI
04048551096628 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

Category: Rigid optical intracranial/spinal endoscope, reusable

Hopkins 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

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Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI d8b063c1-e4d0-4f6f-bd15-5a9b521b4091 33 fields · synced May 30, 2026