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Pressure line

FDA UDI

Class I (US FDA UDI)

by Hamilton Medical, Inc.

Identity

Trade Name
Pressure line FDA UDI
Generic Name
Breathing circuit gas-sampling/monitoring set FDA UDI
Device Name
Pressure line for nCPAP / nCPAP-PC for use with all HAMILTON ventilators, 310 cm, neonatal, single-use FDA UDI
Model / Reference
260176 FDA UDI
Description
Pressure line for nCPAP / nCPAP-PC for use with all HAMILTON ventilators, 310 cm, neonatal, single-use FDA UDI

Identifiers

Primary DI / UDI-DI
07630002804332 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Breathing circuit gas-sampling/monitoring set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Breathing circuit gas-sampling/monitoring set

Pressure line by Hamilton Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit gas-sampling/monitoring set.

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 3a296898-8a0a-47d7-af57-cb2dd0d4cc09 34 fields · synced May 30, 2026