Crawford 28-0172

GUDID M6332801720

Intubation Set Mono-Canalicular Crawford

JEDMED INSTRUMENT COMPANY

Lacrimal intubation set

• Primary Device ID: M6332801720
• NIH Device Record Key: a0b09b8f-4f05-448c-b53d-398ff635b483
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Crawford
• Version Model Number: 28-0172
• Catalog Number: 28-0172
• Company DUNS: 092987189
• Company Name: JEDMED INSTRUMENT COMPANY
• Device Count: 1
• DM Exempt: false
• 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: 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 314-845-3770
• Email: info@jedmed.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M6332801720 [Primary]

FDA Product Code

• OKS: Lacrimal Stents And Intubation Sets

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-12-11
• Device Publish Date: 2016-12-14

On-Brand Devices [Crawford]

• M6332801980: Pigtail Probe Syst Crawford Bellan
• M6332801850: Lacrimal Intubation Set Crawford
• M6332801840: Lacrimal Intubation Set With Suture Crawford
• M6332801750: Lacrimal Intubation Set Crawford II
• M6332801740: Lacrimal Intubation Set With Suture Crawford II
• M6332801720: Intubation Set Mono-Canalicular Crawford