Kolibri RMA108

GUDID 05701780271974

Coloplast A/S

Urological surgical procedure kit, non-medicated, single-use

• Primary Device ID: 05701780271974
• NIH Device Record Key: 9d9ce3fc-4dfb-479b-8ed6-1c193d5d4633
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kolibri
• Version Model Number: RMA108
• Catalog Number: RMA108
• Company DUNS: 305524696
• Company Name: Coloplast A/S
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com
• Phone: +1(800)258-3476
• Email: urology@coloplast.com

Device Dimensions

• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French
• Catheter Gauge: 8 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	05701780271967 [Primary]
GS1	05701780271974 [Package]; Contains: 05701780271967; Package: Retail Box [1 Units]; In Commercial Distribution
GS1	05701780271981 [Package]; Package: Shipper Box [24 Units]; In Commercial Distribution

FDA Product Code

• LJE: CATHETER, NEPHROSTOMY

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: 2024-10-07
• Device Publish Date: 2023-01-20

On-Brand Devices [Kolibri]

• 05701780272186: RMA214
• 05701780272155: RMA212
• 05701780272131: RMA210
• 05701780272100: RMA208
• 05701780272063: RMA114
• 05701780272049: RMA112
• 05701780272001: RMA110
• 05701780271974: RMA108
• 05701780271950: RJB210
• 05701780271912: RJB208
• 05701780271875: RJB110
• 05701780271851: RJB109
• 05701780271813: RJB108
• 05701780271783: RJB007
• 05701780271745: RJB006
• 05701780271714: RJA212
• 05701780271677: RJA210
• 05701780271646: RJA208
• 05701780271622: RJA114
• 05701780271592: RJA112
• 05701780271547: RJA110
• 05701780271509: RJA108
• 05701780271462: RJA008
• 05701780271448: RJA006
• 05701780271417: RCM014
• 05701780271363: RCM012
• 05701780271332: RCM010
• 05701780271318: RCM008
• 05701780271271: RCJ114
• 05701780271240: RCJ112
• 05701780271219: RCJ110
• 05701780271189: RCJ109
• 05701780271165: RCJ108
• 05701780271127: RCJ008
• 05701780271097: RCJ007
• 05701780271066: RCJ006
• 05701780271042: RJD110
• 05701780270977: RJD108
• 05701780270939: RCM020
• 05701780270908: RCM018
• 05701780270878: RCM016