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Velys

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
VELYS FDA UDI
Generic Name
Surgical optical-tracking spatial marker, single-use FDA UDI
Device Name
VELYS SPINE SINGLE INSTRUMENT ARRAY 5 FDA UDI
Model / Reference
451611023 FDA UDI
Description
VELYS SPINE SINGLE INSTRUMENT ARRAY 5 FDA UDI

Identifiers

Catalog Number
451611023 FDA UDI
Primary DI / UDI-DI
10705034643410 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Surgical optical-tracking spatial marker, single-use 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical optical-tracking spatial marker, single-use

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

Similar devices

Also classified as Surgical optical-tracking spatial marker, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b298c44d-f043-42cb-a267-6404ad48a457 34 fields · synced Jun 8, 2026