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Teligen

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
TELIGEN FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
TELIGEN Case Base FDA UDI
Model / Reference
286000000 FDA UDI
Description
TELIGEN Case Base FDA UDI

Identifiers

Catalog Number
286000000 FDA UDI
Primary DI / UDI-DI
10705034548609 FDA UDI
510(k) Number
K212756 FDA UDI
K233254 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df5d7dd3-96b2-46b9-9a1d-c6906540115a 36 fields · synced May 31, 2026