VENA TECH 610771

GUDID 04046964332333

VENA TECH D-PACK VCF ACCESSORY

B. BRAUN MEDICAL INC.

Vena cava filter, permanent

• Primary Device ID: 04046964332333
• NIH Device Record Key: 3befdc6c-4c52-4917-b87d-3815dc4dfe36
• Commercial Distribution Discontinuation: 2026-01-07
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: VENA TECH
• Version Model Number: 610771
• Catalog Number: 610771
• Company DUNS: 002397347
• Company Name: B. BRAUN MEDICAL INC.
• Device Count: 20
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com
• Phone: +1(800)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046964332319 [Unit of Use]
GS1	04046964332333 [Primary]

FDA Product Code

• DTK: FILTER, INTRAVASCULAR, CARDIOVASCULAR

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: 2026-01-08
• Device Publish Date: 2017-01-18

Devices Manufactured by B. BRAUN MEDICAL INC.

• 04046964296697 - Extension Set: 2026-01-15 ANES SET W/DUAL FEM.LL SAFEPORT MANIFOLD
• 04046964183218 - Perifix®: 2026-01-12 PERIFIX® 0.2 µm Flat Epidural Filter - for use with all PERIFIX catheters and PERIFIX PinPad™
• 04046964941054 - PERIFIX™: 2026-01-12 FEF100N FLAT EPIDURAL FILTER NRFIT
• 04046964332333 - VENA TECH: 2026-01-08VENA TECH D-PACK VCF ACCESSORY
• 04046964332333 - VENA TECH: 2026-01-08 VENA TECH D-PACK VCF ACCESSORY
• 04046955672028 - Design Options®: 2025-12-30 NEW ENGLAND BAPTIST HOSPITAL
• 04046955745753 - Introcan Safety ® 2: 2025-12-29 INTROCAN SAFETY 2 W PUR M 24GX14MM - US
• 04046955745838 - Introcan Safety ® 2: 2025-12-29 INTROCAN SAFETY 2 W PUR M 24GX19MM - US
• 04046955745913 - Introcan Safety ® 2: 2025-12-29 INTROCAN SAFETY 2 W PUR M 22GX25MM - US