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Viper

FDA UDI

Class U (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
VIPER FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
VIPER F2 FACET FIXATION SYSTEM SCREW 5 x 40mm FDA UDI
Model / Reference
175710540 FDA UDI
Description
VIPER F2 FACET FIXATION SYSTEM SCREW 5 x 40mm FDA UDI

Identifiers

Catalog Number
175710540 FDA UDI
Primary DI / UDI-DI
10705034034829 FDA UDI
510(k) Number
K101762 FDA UDI
FDA Product Code
MRW FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Spinal bone screw, non-bioabsorbable

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

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

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 c0b77763-224e-42b4-a697-a966621a9290 36 fields · synced Jun 7, 2026