Brachy Needle Box Template B-K D0802002B

GUDID 00801741079153

Brachy Needle Box Template B-K

C. R. Bard, Inc.

General-purpose brachytherapy system applicator, manual

• Primary Device ID: 00801741079153
• NIH Device Record Key: 298ca33f-e2cd-4443-8c20-21b186960cf2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Brachy Needle Box Template B-K
• Version Model Number: D0802002B
• Catalog Number: D0802002B
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• 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: 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

Customer Support Contacts

• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741079153 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972152

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

Sterilization

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

[00801741079153]

Moist Heat or Steam Sterilization

[00801741079153]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-20

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