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Percutaneous Foot Burrs, Arthodesis Burrs

FDA UDI

Class I (US FDA UDI)

by Gm Dos Reis Industria E Comercio Ltda

Identity

Trade Name
Percutaneous Foot Burrs, Arthodesis Burrs FDA UDI
Generic Name
Medullary canal orthopaedic reamer, rigid FDA UDI
Device Name
MIS MICRO BURRS SHANNON LONG Ø2,6x20.0mm FDA UDI
Model / Reference
Burrs Shannon Long FDA UDI
Description
MIS MICRO BURRS SHANNON LONG Ø2,6x20.0mm FDA UDI

Identifiers

Catalog Number
317-07 FDA UDI
Primary DI / UDI-DI
07899258638928 FDA UDI
FDA Product Code
HTT FDA UDI
GMDN Term
Medullary canal orthopaedic reamer, rigid 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medullary canal orthopaedic reamer, rigid

Percutaneous Foot Burrs, Arthodesis Burrs by Gm Dos Reis Industria E Comercio Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medullary canal orthopaedic reamer, rigid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f0200c0-4410-4ecf-8ddc-bf216bf592bc 34 fields · synced May 31, 2026