AccessGUDID - DEVICE: ACTIVDAY (05391512281250)

GUDID

Device Identifier (DI) Information

Brand Name: ACTIVDAY
Version or Model: 501 XL
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 501
Company Name: INDACO SRL

Primary DI Number: 05391512281250
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 338470646 *Terms of Use

Device Description: The ACTIVDAY NO. 501 lumbar-sacral orthosis is designed to support the patient at all stages of his/her recovery. The moldable panels are to be applied post-op without delay for effective immobilization, and kept in place throughout the rehabilitation phase. Later the corset, worn alone, can be adapted to provide comfortable daily support thanks to the progressive immobilization capabilities of our patent pending locking system featuring inter-crossed steps and flexible plastic-covered steel stays. Combined with our comfortable and breathable knitted cotton fabric, you get a result that speaks for itself: Perfect patient compliance. ACTIVDAY NO. 501 consists of 3 separate pieces: A corset fitted with eight (8) flexible steel stays, a covered lumbar thermoplastic panel and an abdominal thermoplastic panel. Indications: • Supports from sacrum to T-9 level. • P ost-op: Following stabilizing surgery, following lumbar disk surgery. • D egenerative pathologies: Osteoporosis, lumbarsacral vertebrae complaint, protrusions, arthritis. • Muscular pathologies: Muscular contractures. • P ractical and easy to fit, it adapts perfectly to your body. • This corset acts as a corrective measure and as a support to postural defects. • Breathable and non allergenic, 100% cotton. • Front panel is 6 3/4” high.

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):	Yes
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?
33031	Lumbar spine orthosis	A prefabricated (non-customized) externally applied and wearable orthopaedic appliance or apparatus designed to encompass the lumbar spine region of the trunk to support or immobilize deformities, fractures, sprains, or strains of the spine. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IPY	Orthosis, Lumbo-Sacral

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: f0fd257f-8a3f-4aed-88c1-e8270c972696
Public Version Date: February 19, 2024
Public Version Number: 1
DI Record Publish Date: February 09, 2024