Plastic Transfer Forceps

GUDID 50628725041549

Plastic Transfer Forceps

Canadian Hospital Specialties Limited

Dressing/utility forceps, tweezers-like, single-use

• Primary Device ID: 50628725041549
• NIH Device Record Key: 75993c44-3db2-46c4-a6a9-d138b5c5ff69
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Plastic Transfer Forceps
• Version Model Number: 85-4200
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• 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
• Phone: 9058259300
• Email: Regulatory.affairs@chsltd.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628725041544 [Primary]
GS1	50628725041549 [Package]; Contains: 00628725041544; Package: Corrugate Case [50 Units]; In Commercial Distribution

FDA Product Code

• HTD: Forceps

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: 2024-04-05
• Device Publish Date: 2024-03-28

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• 50628725095214 - MISI-Medical Imaging Solutions International: 2025-09-19 CT Angiographic Syringe 1 - 200 ml Syringe, 1 - Drip Tubing with Plug, 1 - Large Spike, 1 - Fill Straw, 1 - 60" Y Coiled Tubing