← Back to catalogue

MPM Module (with MR ECG +2 more)

FDA UDIEUDAMED

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name
MPM Module (with MR ECG, NIBP, Temp) FDA UDI
Generic Name
Patient monitoring system module, multifunction FDA UDI
Model / Reference
MPM FDA UDI

Identifiers

Primary DI / UDI-DI
06944904086606 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Patient monitoring system module, multifunction FDA UDI
Models / Variants
with MR ECG FDA UDIEUDAMED
NIBP FDA UDIEUDAMED
Temp FDA UDIEUDAMED

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, multifunction

MPM Module (with MR ECG +2 more) by Shenzhen Mindray Bio-Medical Electronics Co. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — 3 models

Similar devices

Also classified as Patient monitoring system module, multifunction.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 55459e1b-a31c-446a-b32d-67844cfc43de 33 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026