Punch THP154580

GUDID 04250337120452

Punch, straight

Joimax GmbH

Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable Rigid endoscopic biopsy forceps, reusable

• Primary Device ID: 04250337120452
• NIH Device Record Key: be0984c4-03f1-4b7a-a578-6e10378a2f95
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Punch
• Version Model Number: THP154580
• Catalog Number: THP154580
• Company DUNS: 344267187
• Company Name: Joimax GmbH
• 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: 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: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337120452 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

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

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

[04250337120452]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-09
• Device Publish Date: 2023-09-29

Devices Manufactured by Joimax GmbH

• 04250337101338 - guide wire: 2024-02-19 joimax® Guide Wires
• 04250337101369 - guide wire: 2024-02-19 joimax® Guide Wires, PU 5
• 04250337101376 - guide wire: 2024-02-19 joimax® Guide Wire, super elastic, unsterile
• 04250337112440 - guide wire: 2024-02-19 Guide Wire with marker, straight, non-sterile
• 04250337112945 - guide wire: 2024-02-19 joimax® Guide Wire, super elastic, unsterile
• 04250337114154 - guide wire: 2024-02-19 joimax® Guide Wire super elastic, nonsterile
• 04250337114239 - guide wire: 2024-02-19 Guide Wire with markers, straight, non-sterile
• 04250337120124 - Bone Resector: 2023-10-09 Bone Resector, Ball Tip