POST-OP SHOE DLX 1 FEMALE MD

GUDID 00610570137893

Bird & Cronin, LLC

Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis Foot orthosis

• Primary Device ID: 00610570137893
• NIH Device Record Key: 8276efa2-68de-480b-a33c-bce43c7b0a44
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POST-OP SHOE DLX 1 FEMALE MD
• Version Model Number: 50003263
• Company DUNS: 045975349
• Company Name: Bird & Cronin, LLC
• 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: false
• 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	00610570137893 [Primary]

FDA Product Code

• KNP: Orthosis, Corrective Shoe

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-29
• Device Publish Date: 2022-08-20

On-Brand Devices [POST-OP SHOE DLX 1 FEMALE MD]

• 00610570137893: 50003263
• 00610570078929: 08143263