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Viper

FDA UDI

Class I (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
VIPER FDA UDI
Generic Name
Orthopaedic implant aiming/guiding block attachment tool FDA UDI
Device Name
VIPER 2 SYSTEM LARGE DIAMETER LOADING BLOCK FDA UDI
Model / Reference
286705892 FDA UDI
Description
VIPER 2 SYSTEM LARGE DIAMETER LOADING BLOCK FDA UDI

Identifiers

Catalog Number
286705892 FDA UDI
Primary DI / UDI-DI
10705034303437 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant aiming/guiding block attachment tool FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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: Orthopaedic implant aiming/guiding block attachment tool

Viper by Medos International Sàrl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant aiming/guiding block attachment tool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medos International Sàrl

Sources (1)

  • FDA UDI cc8ef8ce-dcaf-45e2-a921-95bbca1a795c 35 fields · synced Jun 6, 2026