Spex Seating

GUDID 09420082699434

6mm T-Slot Assembly

SPEX LIMITED

Wheelchair back rest

• Primary Device ID: 09420082699434
• NIH Device Record Key: 5e3c2a0e-9665-433f-a3f1-5c6278743b36
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spex Seating
• Version Model Number: 0079-0015-000
• Company DUNS: 748649195
• Company Name: SPEX LIMITED
• 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: 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: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com
• Phone: +6433079790
• Email: solutions@spexseating.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	09420082699434 [Primary]

FDA Product Code

• KNN: Components, 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: 2026-03-02
• Device Publish Date: 2026-02-20

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• 09420082699434: 6mm T-Slot Assembly