Solace™ 622517

GUDID 04046964773105

20CC-30ATM INFLATION DEVICE

B BRAUN INTERVENTIONAL SYSTEMS, INC

Catheter/overtube balloon inflator, single-use

• Primary Device ID: 04046964773105
• NIH Device Record Key: 83163c8d-8827-42c6-81be-5ecc67f1d54a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Solace™
• Version Model Number: 622517
• Catalog Number: 622517
• Company DUNS: 784259751
• Company Name: B BRAUN INTERVENTIONAL SYSTEMS, INC
• Device Count: 10
• 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(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(877)836-2228
• Email: GUDID.BBMUS_Service@bbraun.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046964773099 [Unit of Use]
GS1	04046964773105 [Primary]

FDA Product Code

• KOE: DILATOR, URETHRAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2020-05-06
• Device Publish Date: 2016-08-30

Devices Manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC

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• 04046955638406 - ACCEL®: 2024-05-20 ACCEL APD 10F 25CM W/ LOCK
• 04046955638529 - ACCEL®: 2024-05-20 ACCEL APD 12F 25CM W/ LOCK
• 04046955638543 - ACCEL®: 2024-05-20 ACCEL APD 14F 25CM W/ LOCK
• 04046955638567 - ACCEL®: 2024-05-20 ACCEL APD 16F 25CM W/ LOCK
• 04046955638581 - ACCEL®: 2024-05-20 ACCEL APD 8F 25CM W/ MB AND LOCK
• 04046955638604 - ACCEL®: 2024-05-20 ACCEL APD 10F 25CM W/ MB AND LOCK