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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
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI
Device Name
STANDARD NOSE CAP 8.0X1.5X2.0 WITH WIRE FDA UDI
Model / Reference
41-01-06-00 FDA UDI
Description
STANDARD NOSE CAP 8.0X1.5X2.0 WITH WIRE FDA UDI

Identifiers

Primary DI / UDI-DI
07908783000022 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, non-antimicrobial 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: Wound-nonadherent dressing, permeable, non-antimicrobial

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

Similar devices

Also classified as Wound-nonadherent dressing, permeable, non-antimicrobial.

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 8a0e959d-3045-4ea3-b2d5-9084be0d2cc9 33 fields · synced May 31, 2026