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IBP module(FDA/PK.)

FDA UDI

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name
IBP module(FDA/PK.) FDA UDI
Generic Name
Patient monitoring system module, blood pressure, invasive FDA UDI
Model / Reference
115-030774-00 FDA UDI

Identifiers

Primary DI / UDI-DI
06944904086026 FDA UDI
510(k) Number
K153448 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Patient monitoring system module, blood pressure, invasive 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, blood pressure, invasive

IBP module(FDA/PK.) 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, blood pressure, invasive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a6b05961-ef05-492c-b32a-cd4140779fc7 34 fields · synced May 30, 2026