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Stradis

FDA UDI

Class II (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
STRADIS FDA UDI
Generic Name
X-ray film cassette, manual FDA UDI
Device Name
STERILE SEPARATE XRAY CASSETTE COVER FDA UDI
Model / Reference
SS170787 FDA UDI
Description
STERILE SEPARATE XRAY CASSETTE COVER FDA UDI

Identifiers

Primary DI / UDI-DI
M752SS1707870 FDA UDI
FDA Product Code
MMP FDA UDI
GMDN Term
X-ray film cassette, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray film cassette, manual

Stradis by Stradis Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c6518c4-acc9-45a4-a725-cd84696a5356 34 fields · synced Jun 8, 2026