← Back to catalogue

Mindray

FDA UDI

Class I (US FDA UDI)

by GaleMed Xiamen Co., Ltd.

Identity

Trade Name
Mindray FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
Disposable respiratory circuit, Single Limb FDA UDI
Model / Reference
XMR0172 FDA UDI
Description
Disposable respiratory circuit, Single Limb FDA UDI

Identifiers

Catalog Number
040-007123-00 FDA UDI
Primary DI / UDI-DI
06923980111174 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ventilator breathing circuit, single-use

Mindray by GaleMed Xiamen Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

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

Sources (1)

  • FDA UDI 56e4c25f-3c2e-428a-8ad8-5bab87c84583 34 fields · synced May 30, 2026