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Volmed Brasil

FDA UDI

Class I (US FDA UDI)

by Volmed Brasil Equipamentos Ltda

Identity

Trade Name
VOLMED BRASIL FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
EST. CANNULA KIT VOLMED BLOCK 21G X 150MM FDA UDI
Model / Reference
58-01-21-15 FDA UDI
Description
EST. CANNULA KIT VOLMED BLOCK 21G X 150MM FDA UDI

Identifiers

Primary DI / UDI-DI
07908783000305 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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: General surgical procedure kit, non-medicated, 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 General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Volmed Brasil Equipamentos Ltda

Sources (1)

  • FDA UDI 56d46b0b-84e1-4562-a288-4d4cf0be54d0 33 fields · synced May 29, 2026