← Back to catalogue

Expiratory valve set

FDA UDI

Class I (US FDA UDI)

by Hamilton Medical, Inc.

Identity

Trade Name
Expiratory valve set FDA UDI
Generic Name
Mechanical expiratory valve, reusable FDA UDI
Device Name
Expiratory valve set for HAMILTON-C1/T1/MR1, adult/pediatric, autoclavable FDA UDI
Model / Reference
161175 FDA UDI
Description
Expiratory valve set for HAMILTON-C1/T1/MR1, adult/pediatric, autoclavable FDA UDI

Identifiers

Primary DI / UDI-DI
07630002801980 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Mechanical expiratory valve, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Mechanical expiratory valve, reusable

Expiratory valve set by Hamilton Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical expiratory valve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Hamilton Medical, Inc.

Sources (1)

  • FDA UDI e3dae34f-0243-4c3a-9021-464dc605b427 34 fields · synced Jun 8, 2026