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0155 Signal Converter Package(With LED)

FDA UDI

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name
0155 Signal Converter Package(With LED) FDA UDI
Generic Name
Multiple-patient intensive/general healthcare physiologic monitoring system FDA UDI
Model / Reference
115-050747-00 FDA UDI

Identifiers

Primary DI / UDI-DI
06944904098364 FDA UDI
510(k) Number
K162607 FDA UDI
FDA Product Code
MSX FDA UDI
GMDN Term
Multiple-patient intensive/general healthcare physiologic monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Multiple-patient intensive/general healthcare physiologic monitoring system

0155 Signal Converter Package(With LED) by Shenzhen Mindray Bio-Medical Electronics Co. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Multiple-patient intensive/general healthcare physiologic monitoring system.

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 c31cfe4e-b0d1-4d28-966f-8b59321a7c64 34 fields · synced May 30, 2026