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NMT Module (Package/no accessory)

FDA UDIEUDAMED

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name
NMT Module (Package/no accessory) FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Model / Reference
115-044872-00 FDA UDI

Identifiers

Primary DI / UDI-DI
06944904098500 FDA UDI
510(k) Number
K170876 FDA UDI
FDA Product Code
KOI FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2775 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: General-purpose multi-parameter bedside monitor

NMT Module (Package/no accessory) by Shenzhen Mindray Bio-Medical Electronics Co. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 89d24adb-1b48-46ff-86b7-baa43232f2e8 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026