SHAMROCKFLEX FC580SU

GUDID 04046955051984

SHAMROCKFLEX Heart Positioning Device, sterile, disposable

Aesculap AG

Self-retaining surgical retractor, single-use

• Primary Device ID: 04046955051984
• NIH Device Record Key: af26ce60-749c-481e-bb73-cb5a3489c5bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SHAMROCKFLEX
• Version Model Number: FC580SU
• Catalog Number: FC580SU
• Company DUNS: 315018218
• Company Name: Aesculap AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046955051984 [Primary]

FDA Product Code

• MWS: Stabilizer, heart

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-13
• Device Publish Date: 2021-04-05

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• 04038653038244 - AESCULAP: 2025-02-17 Wire Cutting Scissors, straight, 4 1/2", (115 mm), hard wire up to Ø 0.4 mm, non-sterile, reusable
• 04038653038251 - AESCULAP: 2025-02-17 Wire Cutting Scissors, straight, 4 1/2", (115 mm), hard wire up to Ø 0.7 mm, non-sterile, reusable
• 04038653038282 - AESCULAP: 2025-02-17 ANGLE TC Wire Cutting Scissors, straight, 5 1/8", (130 mm), lateral cutting, hard wire up to Ø 0.3 mm, soft wire up to Ø 0.5 m
• 04038653038299 - AESCULAP: 2025-02-17 TC Wire Cutting Scissors, straight, 5 1/8", (130 mm), lateral cutting, hard wire up to Ø 0.4 mm, soft wire up to Ø 0.6 mm, non