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Teligen

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
TELIGEN FDA UDI
Generic Name
Surgical irrigation pump FDA UDI
Device Name
TELIGEN CAMERA WASH BOX US FDA UDI
Model / Reference
286003300 FDA UDI
Description
TELIGEN CAMERA WASH BOX US FDA UDI

Identifiers

Catalog Number
286003300 FDA UDI
Primary DI / UDI-DI
10705034555157 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Surgical irrigation pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation pump

Teligen by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9c14d19-9174-426f-92db-72ea33e411d3 35 fields · synced May 30, 2026