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Djo Surgical

FDA UDI

Class I (US FDA UDI)

by Djo, Llc

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Device Name
ADAPTABLE, UE DISPOSABLE KIT, 5 PACK FDA UDI
Model / Reference
804-33-105 FDA UDI
Description
ADAPTABLE, UE DISPOSABLE KIT, 5 PACK FDA UDI

Identifiers

Primary DI / UDI-DI
00190446667407 FDA UDI
FDA Product Code
IPM FDA UDI
GMDN Term
Arm procedure positioner, reusable 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Arm procedure positioner, reusable

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

Similar devices

Also classified as Arm procedure positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 0da7cfd8-54e0-4752-93bb-537e6c0acb41 33 fields · synced May 30, 2026