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Futuro™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
FUTURO™ FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
FUTURO™ Dress Socks for Men, 71036BLEN, Large, Black FDA UDI
Model / Reference
71036BLEN FDA UDI
Description
FUTURO™ Dress Socks for Men, 71036BLEN, Large, Black FDA UDI

Identifiers

Catalog Number
71036BLEN FDA UDI
Primary DI / UDI-DI
30051131215888 FDA UDI
FDA Product Code
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class
Class II 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, single-use

Futuro™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 3713b78d-843d-4b63-b2ea-a4f57483a6b1 35 fields · synced May 30, 2026