C-Core 19167A Clear View Eye Drape w/Pouch- 19167A

GUDID 00817602021087

EXACT MEDICAL MANUFACTURING, INC.

Patient surgical drape, single-use, sterile

• Primary Device ID: 00817602021087
• NIH Device Record Key: f17a196c-cf10-4ade-9689-8127a1cfa185
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: C-Core 19167A Clear View Eye Drape w/Pouch-
• Version Model Number: 19167A
• Catalog Number: 19167A
• Company DUNS: 014464314
• Company Name: EXACT MEDICAL MANUFACTURING, INC.
• Device Count: 1
• 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: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com
• Phone: 716-681-0866
• Email: rdean@exactmm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817602021070 [Primary]
GS1	00817602021087 [Package]; Contains: 00817602021070; Package: Case [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101598

FDA Product Code

• KKX: Drape, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-08
• Device Publish Date: 2016-09-26

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