Hobbs Biliary Amsterdam Stent Kit 6012

GUDID M84960120

Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.

HOBBS MEDICAL, INC.

Polymeric biliary stent, non-bioabsorbable

• Primary Device ID: M84960120
• NIH Device Record Key: 7bbb30a6-2191-4ab0-84c8-ceb00002779f
• Commercial Distribution Discontinuation: 2024-08-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Hobbs Biliary Amsterdam Stent Kit
• Version Model Number: 6012
• Catalog Number: 6012
• Company DUNS: 076769355
• Company Name: HOBBS MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com
• Phone: 8606845875
• Email: customerservice@hobbsmedical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M84960120 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K834351

FDA Product Code

• FGE: Catheter, Biliary, Diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2026-01-09
• Device Publish Date: 2016-09-21

On-Brand Devices [Hobbs Biliary Amsterdam Stent Kit]

• M84960150: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960140: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960130: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960120: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960110: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960090: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960060: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
• M84960050: Biliary Amsterdam Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.