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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-TEMPERATURE MONITORING KIT FDA UDI
Model / Reference
110-4HMT FDA UDI
Description
MICRO VENTRICULAR BOLT PRESSURE-TEMPERATURE MONITORING KIT FDA UDI

Identifiers

Catalog Number
1104HMT FDA UDI
Primary DI / UDI-DI
00382830047531 FDA UDI
510(k) Number
K962928 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

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

Similar devices

Also classified as Intracerebral sensor catheter, short-term.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Natus Medical Incorporated

Sources (1)

  • FDA UDI e4dcb4b2-5657-47df-9288-e72262b5bc98 37 fields · synced May 30, 2026