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Modus Plan

FDA UDIEUDAMED

Class II (US FDA UDI)

by Synaptive Medical Inc

Identity

Trade Name
Modus Plan FDA UDI
Generic Name
Radiological PACS software FDA UDI
Model / Reference
2.1 FDA UDI

Identifiers

Catalog Number
SYN-0866 FDA UDI
Primary DI / UDI-DI
00670082000511 FDA UDI
510(k) Number
K180394 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Radiological PACS software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiological PACS software

Modus Plan by Synaptive Medical Inc — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Radiological PACS software.

Cleared under the same submission

K180394 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 4a5a2d33-7218-44ca-b672-bf1a39ad5ca6 34 fields · synced Jun 20, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026