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Hamilton-T1

FDA UDI

Class II (US FDA UDI)

by Hamilton Medical, Inc.

Identity

Trade Name
HAMILTON-T1 FDA UDI
Generic Name
Neonatal/adult intensive-care ventilator FDA UDI
Model / Reference
161009 FDA UDI

Identifiers

Catalog Number
161009 FDA UDI
Primary DI / UDI-DI
07630002806091 FDA UDI
FDA Product Code
CBK FDA UDI
BZR FDA UDI
DQA FDA UDI
GMDN Term
Neonatal/adult intensive-care ventilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
868.5330 FDA UDI
870.2700 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Neonatal/adult intensive-care ventilatorTransport electric ventilator

Hamilton-T1 by Hamilton Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transport electric ventilator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hamilton Medical, Inc.

Sources (1)

  • FDA UDI 74210a48-8e79-4e81-8a8a-5aae6406d7f0 33 fields · synced May 30, 2026