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Sedecal

FDA UDI

Class I (US FDA UDI)

by Sedecal., Sa.

Identity

Trade Name
SEDECAL FDA UDI
Generic Name
Diagnostic x-ray system generator, stationary FDA UDI
Device Name
High frequency diagnostic x-ray generator FDA UDI
Model / Reference
SHF-410-C FDA UDI
Description
High frequency diagnostic x-ray generator FDA UDI

Identifiers

Primary DI / UDI-DI
08436046000605 FDA UDI
FDA Product Code
IZO FDA UDI
GMDN Term
Diagnostic x-ray system generator, stationary FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1700 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Diagnostic x-ray system generator, stationary

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

Similar devices

Also classified as Diagnostic x-ray system generator, stationary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sedecal., Sa.

Sources (1)

  • FDA UDI dc6bc029-23c1-4fa0-9838-97b35e9fb637 34 fields · synced Jun 8, 2026