Hegenberger Medical

GUDID 05070000986821

Hegenberger Retractor

HEGENBERGER MEDICAL LIMITED

Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor Post-parturition vaginal retractor

• Primary Device ID: 05070000986821
• NIH Device Record Key: ff8cafc0-751f-458a-bebf-14cf5a4d8249
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hegenberger Medical
• Version Model Number: A13901
• Company DUNS: 228491147
• Company Name: HEGENBERGER MEDICAL LIMITED
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05070000986821 [Primary]

FDA Product Code

• HDL: Retractor, Vaginal

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: 2023-07-06
• Device Publish Date: 2023-06-28