← Back to catalogue

Volmed Brasil

FDA UDI

Class I (US FDA UDI)

by Volmed Brasil Equipamentos Ltda

Identity

Trade Name
VOLMED BRASIL FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
Cutters for Percutaneous Foot Surgery FDA UDI
Model / Reference
BCR70X60XH FDA UDI
Description
Cutters for Percutaneous Foot Surgery FDA UDI

Identifiers

Primary DI / UDI-DI
07908783000299 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, sagittal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

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: Surgical saw blade, sagittal, single-use

Volmed Brasil by Volmed Brasil Equipamentos Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, sagittal, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 38406161-342f-4b63-ad2a-b9d8f2c881f2 33 fields · synced May 30, 2026