DMI

GUDID 10041298501364

Wheelchair Strap Safety Push Button

D-M-S HOLDINGS, INC.

Wheelchair/chair occupant restraint/support

• Primary Device ID: 10041298501364
• NIH Device Record Key: c65d95d7-3434-4909-83b9-88e434ecb05b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DMI
• Version Model Number: 517-5013-0200
• Company DUNS: 062028220
• Company Name: D-M-S HOLDINGS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00041298501367 [Primary]
GS1	10041298501364 [Package]; Contains: 00041298501367; Package: Master carton [100 Units]; In Commercial Distribution

FDA Product Code

• IQB: Belt, Wheelchair

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-19
• Device Publish Date: 2023-07-11

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