AG exhasust gas outlet assembly

FDA UDI

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name: AG exhasust gas outlet assembly FDA UDI
Generic Name: Anaesthesia unit, mobile FDA UDI
Model / Reference: 115-052162-00 FDA UDI

Identifiers

Primary DI / UDI-DI: 06944904000237 FDA UDI
510(k) Number: K171292 FDA UDI
FDA Product Code: BSZ FDA UDI
GMDN Term: Anaesthesia unit, mobile FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5160 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Anaesthesia unit, mobile

AG exhasust gas outlet assembly by Shenzhen Mindray Bio-Medical Electronics Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K171292 also covers:

AG Module(O2/package/accessory) — Shenzhen Mindray Bio-Medical Electronics Co.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co.

Sources (1)

FDA UDI 574d57f3-58fb-4431-bf91-e930c4733ea9 34 fields · synced May 30, 2026