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Sigvaris Magnide on/off

FDA UDI

Class I (US FDA UDI)

by Arion Holding B.V.

Identity

Trade Name
Sigvaris Magnide on/off FDA UDI
Generic Name
Compression/pressure sock/stocking applicator FDA UDI
Device Name
Application aid (donning and doffing) for medical compression garments FDA UDI
Model / Reference
Large FDA UDI
Description
Application aid (donning and doffing) for medical compression garments FDA UDI

Identifiers

Primary DI / UDI-DI
08717127931972 FDA UDI
FDA Product Code
IPM FDA UDI
GMDN Term
Compression/pressure sock/stocking applicator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Compression/pressure sock/stocking applicator

Sigvaris Magnide on/off by Arion Holding B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking applicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arion Holding B.V.

Sources (1)

  • FDA UDI 37cacf30-3bcd-4605-a46a-f7c03f4bf962 33 fields · synced May 30, 2026