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VYRSA General Instrument

FDA UDI

Class I (US FDA UDI)

by Vyrsa Technologies

Identity

Trade Name
VYRSA General Instrument FDA UDI
Generic Name
Orthopaedic chisel FDA UDI
Device Name
Prolix Welded Box Chisel FDA UDI
Model / Reference
VYPR-111-006 FDA UDI
Description
Prolix Welded Box Chisel FDA UDI

Identifiers

Primary DI / UDI-DI
G418VYPR1110060 FDA UDI
FDA Product Code
FZO FDA UDI
GMDN Term
Orthopaedic chisel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 chisel

VYRSA General Instrument by Vyrsa Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vyrsa Technologies

Sources (1)

  • FDA UDI e9bd8699-f744-46e5-a08d-74d52eb17324 33 fields · synced Jun 6, 2026