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Dr Comfort

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
DR COMFORT FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
SS KneeHs OT W 30-40 Nude XL FDA UDI
Model / Reference
702435 FDA UDI
Description
SS KneeHs OT W 30-40 Nude XL FDA UDI

Identifiers

Primary DI / UDI-DI
00888912370059 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, single-use

Dr Comfort by Djo, Llc — 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
Djo, Llc

Sources (1)

  • FDA UDI 60d4c73c-0eaf-48bd-9c8c-2b1cf81a736f 33 fields · synced Jun 1, 2026