Hays Innovations E632203NEO-01N

GUDID 00869566000202

Regular PE Film Probe Cover 6" X 48"

HAYS, INC.

Instrument/equipment drape, single-use, sterile

• Primary Device ID: 00869566000202
• NIH Device Record Key: a09fd543-b2e1-42b4-a2e9-dd4ab9629a17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hays Innovations
• Version Model Number: E632203NEO-01N
• Catalog Number: E632203NEO-01N
• Company DUNS: 079906040
• Company Name: HAYS, 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: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00869566000202 [Primary]
GS1	00869566000219 [Package]; Package: Box [10 Units]; In Commercial Distribution
GS1	00869566000226 [Package]; Contains: 00869566000219; Package: Case [6 Units]; In Commercial Distribution

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-09

On-Brand Devices [Hays Innovations]

• 00869566000264: Hays Ultrasound kit
• 20869566000237: Hays Ultrasound kit
• 00869566000202: Regular PE Film Probe Cover 6" X 48"