LLETZ BAYONET W30

GUDID 00841494103620

LLETZ BAYONET, 15MM LOOP 1/16"

Ellman International

Open-surgery electrosurgical electrode, monopolar, reusable

• Primary Device ID: 00841494103620
• NIH Device Record Key: f59de38e-45d7-4e8f-9bf5-a0dab4484047
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LLETZ BAYONET
• Version Model Number: W30
• Catalog Number: W30
• Company DUNS: 079095245
• Company Name: Ellman International
• Device Count: 1
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841494103620 [Primary]

FDA Product Code

• JOS: Electrode, electrosurgical

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: 2018-03-29
• Device Publish Date: 2016-09-21

On-Brand Devices [LLETZ BAYONET]

• 00841494105242: LLETZ BAYONET, 5MM BALL STERILE
• 00841494105235: LLETZ BAYONET, 25MM LOOP STERILE
• 00841494105228: LLETZ BAYONET, 20MM LOOP STERILE
• 00841494105211: LLETZ BAYONET, 15MM LOOP STERILE
• 00841494103705: LLETZ BAYONET, 8MM ENDO-CERVICAL, 1/16"
• 00841494103682: LLETZ BAYONET, 5MM BALL 1/16"
• 00841494103668: LLETZ BAYONET, 25MM LOOP 1/16"
• 00841494103644: LLETZ BAYONET, 20MM LOOP 1/16"
• 00841494103620: LLETZ BAYONET, 15MM LOOP 1/16"