DEVICE: Invisia™ BathBench (Oil Rubbed Bronze, 30"/762mm, Ash Stain) (00689281031349)

Device Identifier (DI) Information

Invisia™ BathBench (Oil Rubbed Bronze, 30"/762mm, Ash Stain)
INV-WSBB-30-ASH-ORB
In Commercial Distribution
03134
Healthcraft Products Inc.
00689281031349
GS1

1
252468293 *Terms of Use
The Invisia Bath Bench is a high quality, commercial grade bath seat. The Invisia Bath Bench is intended to provide shower seating support for people with reduced mobility. The Invisia Bath Bench rests across the top surface of the bathtub rim, and rubber feet provide friction to reduce horizontal shifting. The maximum user weight for this product is 500lbs / 227kgs. Note: Product is not intended to support full body weight (i.e. do not stand on the seat).The Invisia Bath Bench is not to be used in any other way than described above. The Invisia Bath Bench is made from robust materials and is capable of supporting vigorous forces during proper / normal usage. The structural components of the seat are made from wood (laminated bamboo).
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Device Characteristics

Labeling does not contain MRI Safety Information
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GMDN

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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?
41051 Bath board
A device in the form of a flat board designed to be sat upon by an adult patient who is bathing in a bath (usually while being attended/assisted) to elevate the patient out of the water except for the feet. The patient is typically disabled, infirm, or undergoing medical treatment and cannot sit normally in a bath. The device typically includes a solid or ribbed flat seat and is secured across the rim of the bath; it is typically made of water-resistant or waterproof materials. The device may be used in a hospital, institution, or home.
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FDA Product Code

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Product Code Product Code Name
IKX Aid, Transfer
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FDA Premarket Submission

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

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Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

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Storage and Handling
No storage/handling found
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Clinically Relevant Size

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Size Type Text
No Device Sizes
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Device Record Status

ea6018a5-663f-40b5-a865-02d1c4d00195
September 07, 2021
1
August 30, 2021
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Alternative and Additional Identifiers Additional Identifiers

Package DI

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Secondary DI

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Issuing Agency [?] Secondary DI Number
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Unit of Use DI

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Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

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None
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Production Identifier(s) in UDI

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Customer Contact

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No Customer Contact currently defined
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