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Hummingbird® Patient Monitor

FDA UDI

Class II (US FDA UDI)

by Irras USA

Identity

Trade Name
Hummingbird® Patient Monitor FDA UDI
Generic Name
Intracranial pressure monitor FDA UDI
Device Name
HICP200 Hummingbird Patient / Monitor Interconnect Cable FDA UDI
Model / Reference
HICP200 FDA UDI
Description
HICP200 Hummingbird Patient / Monitor Interconnect Cable FDA UDI

Identifiers

Catalog Number
HICP200 FDA UDI
Primary DI / UDI-DI
00850013266012 FDA UDI
510(k) Number
K161010 FDA UDI
FDA Product Code
GWM FDA UDI
GMDN Term
Intracranial pressure monitor 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Intracranial pressure monitor

Hummingbird® Patient Monitor by Irras USA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intracranial pressure monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Irras USA

Sources (1)

  • FDA UDI abd1e7ec-0355-4e0e-8b5d-92d339fba6cf 37 fields · synced Jun 8, 2026