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Hermann Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by Hermann Medizintechnik GmbH

Identity

Trade Name
Hermann Medizintechnik GmbH FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
Continuous flow Hysteroscopy sheathHigh Flow, ø5,5mm, 5Ch working channelwith stopcock, 2 stopcocks blue,working length 212mm, to use with scope ø 2,9mm 30°, length 303mm FDA UDI
Model / Reference
H51-270-000SH FDA UDI
Description
Continuous flow Hysteroscopy sheathHigh Flow, ø5,5mm, 5Ch working channelwith stopcock, 2 stopcocks blue,working length 212mm, to use with scope ø 2,9mm 30°, length 303mm FDA UDI

Identifiers

Primary DI / UDI-DI
04059453046307 FDA UDI
FDA Product Code
NWW FDA UDI
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1690 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope sheath, reusable

Hermann Medizintechnik GmbH by Hermann Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope sheath, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 64a1c545-df62-4360-aeb9-2c6f549a7ea1 34 fields · synced May 30, 2026