AccessGUDID - DEVICE: M-Brace Air (05391512280161)

GUDID

Device Identifier (DI) Information

Brand Name: M-Brace Air
Version or Model: 16 XL
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 16
Company Name: INDACO SRL

Primary DI Number: 05391512280161
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 338470646 *Terms of Use

Device Description: The ankle brace Strenua – Extra Ankle Lock (#16) is recommended for the diagnosis: Posterior Tibial Tendon Dysfunction; Plantar Fasciitis ; Peroneal tendon instability General mild ankle instability. Indications are: Traumatic pathologies: dislocations – distortions and sub-luxation of the ankle; Rehab phase: passive support for the ankle during late functional rehab phase.: Strongly indicated for use during sport, prevents excessive pronation / supination of the ankle. Thanks to the use of an exclusive, hypo- allergenic and breathable fabric, resulting from a careful research and selection of materials, as well as to the use of a unique construction technology, this ankle-support is extremely comfortable and easy to use. Small sized, it can easily fit any shoe. It can be worn on either foot. Neoprene and latex free.

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):	Yes
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?
44481	Ankle binder, reusable	A strip or roll of fabric or plastic material designed to be wrapped around the ankle to help stabilize and support the joint. It does not include a rigid support (i.e., not an ankle/foot orthosis) and is not a tubular support bandage. This is a reusable device after appropriate cleaning.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FQM	Bandage, Elastic

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: ddbc4c2f-f959-42ce-abe6-9fa5898e086f
Public Version Date: February 05, 2024
Public Version Number: 1
DI Record Publish Date: January 26, 2024