← Back to catalogue

Raypilot Quality Control Kit

FDA UDI

Class II (US FDA UDI)

by Micropos Medical AB (Publ)

Identity

Trade Name
Raypilot Quality Control Kit FDA UDI
Generic Name
Radiation therapy invasive marker lesion localization system FDA UDI
Device Name
Raypilot Quality Control Kit is aimed to be used for daily quality control prior to any treatment. FDA UDI
Model / Reference
1 FDA UDI
Description
Raypilot Quality Control Kit is aimed to be used for daily quality control prior to any treatment. FDA UDI

Identifiers

Catalog Number
4005 FDA UDI
Primary DI / UDI-DI
07350007954053 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 Quality Control Kit 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d455781a-b2f3-4da2-aec6-fca98c67a70f 38 fields · synced May 30, 2026