AccessGUDID - DEVICE: Reflex (00860013061104)

GUDID

Device Identifier (DI) Information

Brand Name: Reflex
Version or Model: KN33-LE
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Assistive Technology Development, Inc.

Primary DI Number: 00860013061104
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 119319634 *Terms of Use

Device Description: Reflex is a rehabilitative exercise device that fits to the lower limb and is intended to facilitate knee stretching and strengthening exercises and perform measurement functions for rehabilitation related to musculoskeletal pathologies, injury, and/or surgery of the knee. Reflex is intended to be used in a clinical or home environment.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
60926	Virtual-display rehabilitation system, non-supportive, home-use	An assembly of devices intended to be used both in a home and clinical setting and to provide non-gravity-compensating rehabilitation therapy for neuromuscular/musculoskeletal conditions affecting the back, trunk, and/or limbs (e.g., impaired limb function) through patient interaction with a videogame-like display prompting repeated motion of a body part (e.g., arm, hand, leg) for functional improvement; it may also provide performance feedback. It does not provide weight support and is based on motion-sensing devices [e.g., patient-worn infrared (IR) glove, motion tracking heel pad or camera, software] that communicate to provide a virtual-display interface.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IKK	System, Isokinetic Testing And Evaluation

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 045e54e5-3006-49d3-9db8-a72b95e53a2b
Public Version Date: May 01, 2025
Public Version Number: 1
DI Record Publish Date: April 23, 2025