Camino®

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name: CAMINO® FDA UDI
Generic Name: Intracerebral sensor catheter, short-term FDA UDI
Device Name: MICRO VENTRICULAR BOLT PRESSURE MONITORING KIT FDA UDI
Model / Reference: 110-4HM FDA UDI
Description: MICRO VENTRICULAR BOLT PRESSURE MONITORING KIT FDA UDI

Identifiers

Catalog Number: 1104HM FDA UDI
Primary DI / UDI-DI: 00382830047524 FDA UDI
510(k) Number: K914735 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Intracerebral sensor catheter, short-term

Camino® by Natus Medical Incorporated — 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: Natus Medical Incorporated

Sources (1)

FDA UDI 39ad3aef-e865-436f-9c56-3ceef2b73048 37 fields · synced Jun 8, 2026