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Air hose

FDA UDI

Class II (US FDA UDI)

by CNSystems Medizintechnik GmbH

Identity

Trade Name
Air hose FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Unit; 2.5m, Air hose for Task Force® Monitor incl. 2x Rectus connector FDA UDI
Model / Reference
V1.0 FDA UDI
Description
Unit; 2.5m, Air hose for Task Force® Monitor incl. 2x Rectus connector FDA UDI

Identifiers

Catalog Number
00060 FDA UDI
Primary DI / UDI-DI
09120073931788 FDA UDI
510(k) Number
K014063 FDA UDI
FDA Product Code
DSB FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 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

No

FDA UDI

Category: General-purpose multi-parameter bedside monitor

Air hose by CNSystems Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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 8c85e9e9-90f1-4d67-81cc-113d8f15c560 37 fields · synced May 30, 2026