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Raypilot System Cable

FDA UDI

Class II (US FDA UDI)

by Micropos Medical AB (Publ)

Identity

Trade Name
Raypilot System Cable FDA UDI
Generic Name
Radiation therapy invasive marker lesion localization system FDA UDI
Device Name
Cable connecting the Raypilot Power box to the Raypilot Receiver FDA UDI
Model / Reference
1 FDA UDI
Description
Cable connecting the Raypilot Power box to the Raypilot Receiver FDA UDI

Identifiers

Catalog Number
6002 FDA UDI
Primary DI / UDI-DI
07350007956026 FDA UDI
510(k) Number
K203722 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiation therapy invasive marker lesion localization system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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: Radiation therapy invasive marker lesion localization system

Raypilot System Cable by Micropos Medical AB (Publ) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy invasive marker lesion localization system.

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 1556b799-a090-49b8-9004-d653797fbca9 36 fields · synced May 30, 2026