ORCA Foam Powder

GUDID 00850056665131

AbsorbaleGelatin Powder

Orca Products, LLC

Gelatin haemostatic agent

• Primary Device ID: 00850056665131
• NIH Device Record Key: 359622a6-954f-4fcb-9012-a7edfa63bc06
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ORCA Foam Powder
• Version Model Number: OF-03B
• Company DUNS: 117716283
• Company Name: Orca Products, LLC
• Device Count: 6
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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

Customer Support Contacts

• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com
• Phone: 334-803-2370
• Email: cdsdds@me.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850056665131 [Unit of Use]
GS1	00850056665148 [Primary]

FDA Product Code

• LYA: Splint, Intranasal Septal

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: 2024-12-13
• Device Publish Date: 2024-12-05

On-Brand Devices [ORCA Foam Powder]

• 00850056665131: AbsorbaleGelatin Powder
• 00850056665117: AbsorbaleGelatin Powder
• 00850056665094: AbsorbaleGelatin Powder
• 10850056665244: "AbsorbaleGelatin Powder--Pre-filled 1g Syringe "