STRAP, ULTRA SHOULDER CHIN 5345-5

GUDID 00842430101762

MIZUHO ORTHOPEDIC SYSTEMS, INC.

Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use Limb/torso/head restraint, single-use

• Primary Device ID: 00842430101762
• NIH Device Record Key: 47f05a4b-9bbd-4ce5-86a6-6759cb0d9ef7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STRAP, ULTRA SHOULDER CHIN
• Version Model Number: 5345-5
• Catalog Number: 5345-5
• Company DUNS: 084527241
• Company Name: MIZUHO ORTHOPEDIC SYSTEMS, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: 800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842430101762 [Primary]

FDA Product Code

• FMQ: Restraint, Protective

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: 2023-09-04
• Device Publish Date: 2023-08-25

Devices Manufactured by MIZUHO ORTHOPEDIC SYSTEMS, INC.

• 00842430116322 - AQUARI IMMERSION CONTROLLER REFURB: 2024-03-15
• 00842430113727 - FOOT SUPPORT ASSEMBLY: 2024-03-14
• 00842430101212 - Pad Set For GST Tempur-Pedic, 76MM: 2023-09-27
• 00842430101311 - SPAR,LEG,RIGHT RADIOLUCENT,REFURBISHED: 2023-09-27
• 00842430101328 - SPAR, LEG, LEFT, RADIOLUCENT, REFURBISHED: 2023-09-27
• 00842430101335 - SPAR ASSEMBLY, RIGHT, REFURBISHED: 2023-09-27
• 00842430101342 - SPAR ASSEMBLY, LEFT, REFURBISHED: 2023-09-27
• 00842430103414 - UPPER ARM SUPPORT & PAD, REFURBISHED: 2023-09-27