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CAPNOSTAT CO2(Package/no accessory)

FDA UDI

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name
CAPNOSTAT CO2(Package/no accessory) FDA UDI
Generic Name
Patient monitoring system module, carbon dioxide FDA UDI
Model / Reference
115-013200-00 FDA UDI

Identifiers

Primary DI / UDI-DI
06944904085821 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Patient monitoring system module, carbon dioxide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Patient monitoring system module, carbon dioxide

CAPNOSTAT CO2(Package/no accessory) by Shenzhen Mindray Bio-Medical Electronics Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, carbon dioxide.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shenzhen Mindray Bio-Medical Electronics Co.

Sources (1)

  • FDA UDI 5f97a2be-54bc-4fb9-a2a9-244fd653a756 33 fields · synced Jun 6, 2026