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Contec

FDA UDI

Class II (US FDA UDI)

by Contec Medical Systems Co., Ltd.

Identity

Trade Name
CONTEC FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Patient Monitor FDA UDI
Model / Reference
PM50 FDA UDI
Description
Patient Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
06945040100522 FDA UDI
510(k) Number
K101127 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor 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

No

FDA UDI

Category: General-purpose multi-parameter bedside monitor

Contec by Contec Medical Systems Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd0db227-b5de-48dd-afa9-55168bed3766 34 fields · synced Jun 8, 2026