FEATHER SURGICAL BLADE STAINLESS STEEL

GUDID 04902470017693

FEATHER SAFETY RAZOR CO., LTD.

Manual scalpel blade, single-use

• Primary Device ID: 04902470017693
• NIH Device Record Key: 77e55292-e2e4-402f-963b-0d9e09f75f0e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FEATHER SURGICAL BLADE STAINLESS STEEL
• Version Model Number: No.12d
• Company DUNS: 690555024
• Company Name: FEATHER SAFETY RAZOR CO., LTD.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04902470017693 [Primary]

FDA Product Code

• GES: Blade, 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: 2022-08-09
• Device Publish Date: 2022-08-01

On-Brand Devices [FEATHER SURGICAL BLADE STAINLESS STEEL]

• 04902470017914: No.391
• 04902470017907: No.350
• 04902470017815: No.390C
• 04902470017747: No.390
• 04902470017716: No.370
• 04902470017693: No.12d
• 04902470017686: No.14
• 04902470017655: No.15C
• 04902470017648: No.25
• 04902470017631: No.24
• 04902470017624: No.23
• 04902470017617: No.22
• 04902470017600: No.21
• 04902470017594: No.20
• 04902470017587: No.15
• 04902470017570: No.12
• 04902470017563: No.11
• 04902470017556: No.10