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Donjoy

FDA UDI

Class I (US FDA UDI)

by Djo, Llc

Identity

Trade Name
DONJOY FDA UDI
Generic Name
Assistive sock/pantyhose dressing device FDA UDI
Device Name
DRESSING,UNIVERSAL,XL, STERILE FDA UDI
Model / Reference
11-0823-9-00000 FDA UDI
Description
DRESSING,UNIVERSAL,XL, STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
00888912152556 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Assistive sock/pantyhose dressing device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Assistive sock/pantyhose dressing device

Donjoy by Djo, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive sock/pantyhose dressing device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI bdddfaee-508e-4d23-b3b5-6e8d2f97c876 33 fields · synced May 30, 2026