CESSYS® CER112835

GUDID 04250337105152

CESSYS® Cervical Reamer

Joimax GmbH

Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use

• Primary Device ID: 04250337105152
• NIH Device Record Key: 54b7050e-bc9d-404b-8940-78d174afa4e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CESSYS®
• Version Model Number: CER112835
• Catalog Number: CER112835
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: +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
• 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 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	04250337105145 [Primary]
GS1	04250337105152 [Package]; Contains: 04250337105145; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• HTO: REAMER

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: 2023-09-13
• Device Publish Date: 2022-12-30

On-Brand Devices [CESSYS®]

• 04250337114697: CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo
• 04250337114680: CESSYS® Dorsal FHD Laminoscope (4.7 WCh), ocular
• 04250337105879: CESSYS® Cervical Hybrid Scope, combo
• 04250337116837: CESSYS® Dorsal DIN-Norm-Container, yellow Lid
• 04250337108818: CESSYS® DIN-Norm-Container, gold Lid
• 04250337105152: CESSYS® Cervical Reamer