← Back to catalogue

Solidea

FDA UDI

Class I (US FDA UDI)

by Calzificio Pinelli Srl

Identity

Trade Name
SOLIDEA FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
MARILYN 70 SHEER OPEN TOE, SIZE ML, NERO, GRADUATED COMPRESSION 12/15 mmHg SHEER STAY UP STOCKING WITH SILICONE BAND AND OPEN FLIP-FLOP DESIGN FDA UDI
Model / Reference
054535 FDA UDI
Description
MARILYN 70 SHEER OPEN TOE, SIZE ML, NERO, GRADUATED COMPRESSION 12/15 mmHg SHEER STAY UP STOCKING WITH SILICONE BAND AND OPEN FLIP-FLOP DESIGN FDA UDI

Identifiers

Catalog Number
051870 FDA UDI
Primary DI / UDI-DI
08300496054535 FDA UDI
FDA Product Code
FQL FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5780 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

No

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

Category: Compression/pressure sock/stocking, reusable

Solidea by Calzificio Pinelli Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d0109864-b15d-46a6-9944-2674c3039476 34 fields · synced Jun 6, 2026