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Medstone

FDA UDI

Class II (US FDA UDI)

by Stille AB

Identity

Trade Name
Medstone FDA UDI
Generic Name
Fluoroscopy/angiography table, powered FDA UDI
Device Name
Examination and procedure table FDA UDI
Model / Reference
Medstone3 PM FDA UDI
Description
Examination and procedure table FDA UDI

Identifiers

Catalog Number
500-1005 FDA UDI
Primary DI / UDI-DI
07332339226541 FDA UDI
FDA Product Code
IXR FDA UDI
GMDN Term
Fluoroscopy/angiography table, powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluoroscopy/angiography table, powered

Medstone by Stille AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluoroscopy/angiography table, powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 4d6c14d9-4a81-476a-bfed-ac6e6655b129 35 fields · synced Jun 1, 2026