DEVICE: DONDOLINO (08055715705506)
Device Identifier (DI) Information
DONDOLINO
DONDOLINO 2
In Commercial Distribution
ORMESA SRL
DONDOLINO 2
In Commercial Distribution
ORMESA SRL
Tilting vertical standing frame indicated for the acquisition and maintenance of an upright position and the training of the antigravity muscles of children who cannot acquire and maintain them independently. Indicated for users suffering from pathologies that determine a deficit of postural control, in which the load of the lower limbs is still allowed, to improve bone density, ventilatory capacity, intestinal peristalsis, bladder function, blood circulation and for such as the semi-prone positioning, allows to stimulate the straightening reactions of the trunk and head and to work against gravity.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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61700 | Manual stander |
A manually-powered, mobile device designed to support and lift a disabled (paraplegic) patient to an upright standing position to provide the health benefits associated with standing (e.g., improved breathing, circulation, and flexibility); it is neither intended to facilitate gait nor assist standing transfer. It typically consists of a seat, sling and/or platform with appropriate supports (e.g., footplates, kneepads, chest pad), wheels, and a manual mechanical lifting mechanism whereby the patient is raised from a supine, prone, and/or seated position by themselves or with the assistance of a healthcare provider. It includes wheels for reorientation.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
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INM | Chair, With Casters |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
71d48af7-0597-4251-b7f8-0ffa3d9cfaac
February 10, 2025
1
January 31, 2025
February 10, 2025
1
January 31, 2025
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined