Lateral Clamp 16577GY

GUDID 04251388900321

adeor Medical AG

Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps

• Primary Device ID: 04251388900321
• NIH Device Record Key: d2e1ae61-197b-4cbe-a119-4120261e9ec8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lateral Clamp
• Version Model Number: sideways curved 240 mm
• Catalog Number: 16577GY
• Company DUNS: 341188943
• Company Name: adeor Medical AG
• Device Count: 1
• DM Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04251388900321 [Primary]

FDA Product Code

• KOH: Instrument, Manual, General Obstetric-Gynecologic

Sterilization

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

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

[04251388900321]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-09
• Device Publish Date: 2020-09-01

Devices Manufactured by adeor Medical AG

• 04251388960455 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960462 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960479 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960547 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960554 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960561 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960578 - nxt™ Bipolar Forceps: 2023-05-31
• 04251388960585 - nxt™ Bipolar Forceps: 2023-05-31