KEMIS

GUDID 03700569660000

KEMIS H3 Knife

NEWCLIP TECHNICS

Scalpel, single-use

• Primary Device ID: 03700569660000
• NIH Device Record Key: 93f183e4-5a4a-490f-8469-ea463c546a31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KEMIS
• Version Model Number: ANC209
• Company DUNS: 263281904
• Company Name: NEWCLIP TECHNICS
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700569611712 [Primary]
GS1	03700569660000 [Package]; Contains: 03700569611712; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• GDZ: Handle, Scalpel

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: 2025-12-18
• Device Publish Date: 2025-12-10

On-Brand Devices [KEMIS]

• 03700569660017: ANC1103
• 03700569660000: KEMIS H3 Knife