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Mindray > Datascope Compatible NIBP Hose

FDA UDI

Class II (US FDA UDI)

by Cables And Sensors, Llc

Identity

Trade Name
Mindray > Datascope Compatible NIBP Hose FDA UDI
Generic Name
Invasive blood pressure monitoring tubing set FDA UDI
Model / Reference
10572 FDA UDI

Identifiers

Primary DI / UDI-DI
B817105720 FDA UDI
510(k) Number
K173197 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Invasive blood pressure monitoring tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Invasive blood pressure monitoring tubing set

Mindray > Datascope Compatible NIBP Hose by Cables And Sensors, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive blood pressure monitoring tubing set.

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 651f6f6b-5f0e-4028-8b85-08c3705917fa 33 fields · synced May 31, 2026