SHEFA Forcep

GUDID 00860008457431

FORCEPS, BIOPSY, NON-ELECTRIC

Shefa Solutions Inc.

Flexible endoscopic biopsy forceps, single-use

• Primary Device ID: 00860008457431
• NIH Device Record Key: 735d5435-507b-4d67-b84a-edc65bf254d9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SHEFA Forcep
• Version Model Number: 1
• Company DUNS: 118646521
• Company Name: Shefa Solutions Inc.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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	00860008457400 [Primary]
GS1	00860008457424 [Package]; Package: Outer Box [10 Units]; In Commercial Distribution
GS1	00860008457431 [Package]; Contains: 00860008457400; Package: Inner Box [10 Units]; In Commercial Distribution

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: 2022-05-09
• Device Publish Date: 2022-04-29

Devices Manufactured by Shefa Solutions Inc.

• 00860008457431 - SHEFA Forcep: 2022-05-09FORCEPS, BIOPSY, NON-ELECTRIC
• 00860008457431 - SHEFA Forcep: 2022-05-09 FORCEPS, BIOPSY, NON-ELECTRIC
• 10860008457414 - SHEFA Block: 2022-05-09