AccessGUDID - DEVICE: M-Brace Air (05391512280123)

GUDID

Device Identifier (DI) Information

Brand Name: M-Brace Air
Version or Model: 15 R
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 15
Company Name: INDACO SRL

Primary DI Number: 05391512280123
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 338470646 *Terms of Use

Device Description: The Mercurio Ankle Lock brace, with elastic, reinforced strap to be applied to the ankle using our locking system. In order to ensure maximum comfort and tolerance, especially in the case of extended use, particular care and attention have been dedicated to the selection of materials and fabrics. As such, our products are made exclusively with all natural, hypo-allergenic and breathable fibers. The inside fabric of this product is the result of a unique technology. It is made with very soft cotton velour providing the skin with an extremely comfortable touch and at the same time, allowing it to breathe freely all day-even while playing sports.

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: 03c7aac4-8922-401d-b9d3-8d5d65b56059
Public Version Date: February 05, 2024
Public Version Number: 1
DI Record Publish Date: January 26, 2024