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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 laryngopharyngoscope FDA UDI
Device Name
HOPKINS® Telescope 0°, 5.8mm, 19cm FDA UDI
Model / Reference
8710AA FDA UDI
Description
HOPKINS® Telescope 0°, 5.8mm, 19cm FDA UDI

Identifiers

Primary DI / UDI-DI
04048551216552 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 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 laryngopharyngoscope

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 laryngopharyngoscope.

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 276b6bdb-d4bd-4df4-b7e9-f3872baf79db 33 fields · synced May 30, 2026