← Back to catalogue

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
Medstone2 PM FDA UDI
Description
Examination and procedure table FDA UDI

Identifiers

Catalog Number
500-1011 FDA UDI
Primary DI / UDI-DI
07332339226589 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

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

Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 5eb02e13-57ac-4279-9206-f85d6ab32845 35 fields · synced May 30, 2026