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Trialtis

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
TRIALTIS FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
TRIALTIS Spine System Lateral Connector Caddy Fixed FDA UDI
Model / Reference
5161016000 FDA UDI
Description
TRIALTIS Spine System Lateral Connector Caddy Fixed FDA UDI

Identifiers

Catalog Number
5161016000 FDA UDI
Primary DI / UDI-DI
10705034597911 FDA UDI
510(k) Number
K243249 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Trialtis 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 1f9ad08e-23c1-4637-a8a7-334962a22399 36 fields · synced May 30, 2026