SUTURE REMOVAL KIT 8520

GUDID 50628725005374

SUTURE REMOVAL KIT

Canadian Hospital Specialties Limited

Suture removal kit

• Primary Device ID: 50628725005374
• NIH Device Record Key: 5511c695-4558-4d3c-9883-704a60290201
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUTURE REMOVAL KIT
• Version Model Number: 8520
• Catalog Number: 8520
• Company DUNS: 240992693
• Company Name: Canadian Hospital Specialties 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com
• Phone: 9058259300
• Email: regulatory.affairs@chsltd.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628725005379 [Primary]
GS1	50628725005374 [Package]; Contains: 00628725005379; Package: CORRUGATE [50 Units]; In Commercial Distribution

FDA Product Code

• MCZ: Suture Removal Kit

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-10
• Device Publish Date: 2025-06-02

Devices Manufactured by Canadian Hospital Specialties Limited

• 50628725005374 - SUTURE REMOVAL KIT: 2025-06-10SUTURE REMOVAL KIT
• 50628725005374 - SUTURE REMOVAL KIT: 2025-06-10 SUTURE REMOVAL KIT
• 00628725002200 - MED-RX: 2025-05-05 CONN TUBE STERILE 1/4 X 120"
• 50628725002229 - MED-RX: 2025-05-05 CONN TUBE STERILE 1/4 X 180" SPECIAL
• 50628725002236 - MED-RX: 2025-05-05 CONN TUBE STERILE 1/4 X 240"
• 50628725095290 - MiniMuffs: 2025-04-21
• 00628725008264 - Smart Scale: 2025-03-10 Smart Scale
• 00628725008271 - SMART SCALE: 2025-03-10 Smart Scale
• 50628725099694 - ADULT AEROSOL MASK WITH 7FT SAFLO TUBE: 2025-02-21 ADULT AEROSOL MASK WITH 7FT SAFLO TUBE