BeneCath®

GUDID 06972624970011

Hangzhou Jimushi Meditech Co., Ltd.

Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use Intermittent urethral drainage catheter, non-antimicrobial, single-use

• Primary Device ID: 06972624970011
• NIH Device Record Key: c2be19f2-defe-48c5-b5ff-f2d04bae75c6
• Commercial Distribution Discontinuation: 2020-12-17
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: BeneCath®
• Version Model Number: NC08M
• Company DUNS: 413190154
• Company Name: Hangzhou Jimushi Meditech Co., Ltd.
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972624970011 [Package]; Contains: 16972624970018; Package: BOX [30 Units]; Discontinued: 2020-12-17; Not in Commercial Distribution
GS1	16972624970018 [Primary]
GS1	26972624970015 [Package]; Package: CARTON [10 Units]; Discontinued: 2020-12-17; Not in Commercial Distribution

FDA Product Code

• GBM: Catheter, 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: 2
• Public Version Date: 2020-12-18
• Device Publish Date: 2020-11-10

On-Brand Devices [BeneCath®]

• 16972624970049: NCW14M
• 06972624970011: NC08M
• 06972624970714: NC16P
• 06972624970707: NC14P
• 06972624970691: NC12P
• 06972624970684: NC10P
• 06972624970677: NC08P
• 06972624970653: NC16F
• 06972624970646: NC14F
• 06972624970639: NC12F
• 06972624970622: NC10F
• 06972624970615: NC08F
• 06972624970608: NC18MC
• 06972624970592: NC16MC
• 06972624970585: NC14MC
• 06972624970578: NC12MC
• 06972624970561: NC10MC
• 06972624970554: NC08MC
• 06972624970547: NC18M
• 06972624970530: NC16M
• 06972624970523: NC14M
• 06972624970516: NC12M
• 06972624970509: NC10M
• 06972624970493: NC08M
• 06972624970417: NCH16F
• 06972624970400: NCH14F
• 06972624970394: NCH12F
• 06972624970387: NCH10F
• 06972624970363: NCH18MC
• 06972624970356: NCH16MC
• 06972624970349: NCH14MC
• 06972624970332: NCH12MC
• 06972624970325: NCH10MC
• 06972624970301: NCH18M
• 06972624970295: NCH16M
• 06972624970288: NCH14M
• 06972624970271: NCH12M
• 06972624970264: NCH10M
• 06972624970257: NCH08M
• 06972624970202: NCW10P
• 06972624970196: NCW08P
• 06972624970189: NCW18F
• 06972624970172: NCW16F
• 06972624970165: NCW14F
• 06972624970158: NCW12F
• 06972624970141: NCW10F
• 06972624970134: NCW08F
• 06972624970127: NCW18MC
• 06972624970110: NCW16MC
• 06972624970103: NCW14MC