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Sedecal

FDA UDI

Class II (US FDA UDI)

by Sedecal., Sa.

Identity

Trade Name
SEDECAL FDA UDI
Generic Name
Basic diagnostic x-ray system table, powered FDA UDI
Device Name
Stationary diagnostic x-ray table FDA UDI
Model / Reference
MULT-FWFTTD FDA UDI
Description
Stationary diagnostic x-ray table FDA UDI

Identifiers

Primary DI / UDI-DI
08436046002937 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Basic diagnostic x-ray system 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic diagnostic x-ray system table, powered

Sedecal by Sedecal., Sa. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic diagnostic x-ray system table, powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sedecal., Sa.

Sources (1)

  • FDA UDI 26e79187-f0da-49c5-a9da-6bcb469194c6 34 fields · synced May 31, 2026