Neurovent-Ifd-S

FDA UDI

Class II (US FDA UDI)

by Raumedic Ag

Identity

Trade Name: NEUROVENT-IFD-S FDA UDI
Generic Name: Intracerebral sensor catheter, short-term FDA UDI
Model / Reference: 091678-002 FDA UDI

Identifiers

Primary DI / UDI-DI: 04057834024753 FDA UDI
FDA Product Code: GWM FDA UDI
GMDN Term: Intracerebral sensor catheter, short-term FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1620 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 3.10 Millimeter FDA UDI

Category: Intracerebral sensor catheter, short-term

Neurovent-Ifd-S by Raumedic Ag — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Raumedic Ag

Sources (1)

FDA UDI 19fbb112-b725-4db6-bef7-1ddeb8c88b08 35 fields · synced Jun 6, 2026