PERIFIX™ 339163

GUDID 04046964941115

PCC1900N 19GA CATH CONN NRFIT

B. BRAUN MEDICAL INC.

NRFit/non-ISO80369-standardized linear connector

• Primary Device ID: 04046964941115
• NIH Device Record Key: a3f3d7af-c825-4f69-ab7e-50fcd6fb4731
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERIFIX™
• Version Model Number: 339163
• Catalog Number: 339163
• Company DUNS: 002397347
• Company Name: B. BRAUN MEDICAL INC.
• Device Count: 50
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046964941108 [Unit of Use]
GS1	04046964941115 [Primary]

FDA Product Code

• CAZ: Anesthesia conduction kit

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: 2020-03-03
• Device Publish Date: 2016-11-06

On-Brand Devices [PERIFIX™]

• 04046964941139: PCC2000N 20GA - 24GA CATH CONN NRFIT
• 04046964941115: PCC1900N 19GA CATH CONN NRFIT
• 04046955735471: PERIFIX 10 ML GLASS LOR SYR LOCK NRFIT
• 04046955735457: PERIFIX 10 ML GLASS LOR SYR SLIP NRFIT
• 04046955768233: 18GA X 4.75 TOUHY NEEDLE EPIDURAL-NRFIT