STRAP UNIVERSAL 4IN x 72IN 10/PK 2970009996

GUDID 00733657283624

ALIMED, INC.

Limb/torso/head restraint, reusable

• Primary Device ID: 00733657283624
• NIH Device Record Key: 08bb7244-265b-40a4-b673-f567ea620604
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STRAP UNIVERSAL 4IN x 72IN 10/PK
• Version Model Number: 753910
• Catalog Number: 2970009996
• Company DUNS: 056007248
• Company Name: ALIMED, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com
• Phone: +1(781)329-2900
• Email: customerservice@alimed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00733657283624 [Primary]
GS1	00733657300192 [Unit of Use]

FDA Product Code

• CCX: SUPPORT, PATIENT POSITION

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-19
• Device Publish Date: 2022-12-15

Devices Manufactured by ALIMED, INC.

• 00733657301038 - ATEC KIT 4 STRAPS: 2024-08-12
• 00733657288667 - ATEC STRAP 2 X 84IN 2 CLOSURE PELVIC LONG: 2024-08-12
• 00733657288674 - ATEC STRAP 2 X 72IN 2 CLOSURE PELVIC SHORT: 2024-08-12
• 00733657288681 - ATEC STRAP 2 X 42IN 2 CLOSURE THORACIC: 2024-08-12
• 00733657230253 - CUSH DROP AWAY POMMEL 16X16: 2024-02-19
• 00733657230260 - DROP AWAY POMMEL CUSHION 18X16: 2024-02-19
• 00733657240054 - CATH LAB IMMOBILIZER: 2024-02-19
• 00733657245035 - STRAP UNIVERSAL UNIBODY, 5WX65L: 2024-02-19