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MEDRAD® XDS Patient Interface Disposable

FDA UDI

Class I (US FDA UDI)

by Bayer Medical Care Inc.

Identity

Trade Name
MEDRAD® XDS Patient Interface Disposable FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
XDS Patient Interface Disposable (CT - EXTRAVASATION PID) (60727773) FDA UDI
Model / Reference
XDS PID FDA UDI
Description
XDS Patient Interface Disposable (CT - EXTRAVASATION PID) (60727773) FDA UDI

Identifiers

Catalog Number
XDS PID FDA UDI
Primary DI / UDI-DI
00616258005409 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Adhesive bandage

MEDRAD® XDS Patient Interface Disposable by Bayer Medical Care Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8679b968-7fbf-40a9-a694-62a8f1b8e0cf 35 fields · synced Jun 9, 2026