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External Drainage Monitoring

FDA UDI

Class II (US FDA UDI)

by Medtronic PS Medical

Identity

Trade Name
EXTERNAL DRAINAGE MONITORING FDA UDI
Generic Name
Ventricular cerebrospinal fluid drainage catheterization kit FDA UDI
Device Name
KIT 27297 EDM DRAINAG VENT CATH FDA UDI
Model / Reference
27297 FDA UDI
Description
KIT 27297 EDM DRAINAG VENT CATH FDA UDI

Identifiers

Primary DI / UDI-DI
00763000406059 FDA UDI
FDA Product Code
GWN FDA UDI
GMDN Term
Ventricular cerebrospinal fluid drainage catheterization kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1460 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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: Ventricular cerebrospinal fluid drainage catheterization kit

External Drainage Monitoring by Medtronic PS Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventricular cerebrospinal fluid drainage catheterization kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16e81afe-aa31-448b-810e-f920a3dbc9f6 34 fields · synced May 30, 2026