Platinum Code

GUDID 00810034800862

IPC, INC.

Nitrile examination/treatment glove, non-powdered, non-sterile

• Primary Device ID: 00810034800862
• NIH Device Record Key: 54d88ce7-5e9a-47b0-b8eb-f8558d38daed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Platinum Code
• Version Model Number: 2039NB-M
• Company DUNS: 832991392
• Company Name: IPC, INC.
• Device Count: 200
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810034800862 [Primary]
GS1	00810034800978 [Unit of Use]

FDA Product Code

• LZA: Polymer Patient Examination Glove

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: 2020-02-17
• Device Publish Date: 2020-02-07

On-Brand Devices [Platinum Code]

• 00810034800886: 2039NB-XL
• 00810034800879: 2039NB-L
• 00810034800862: 2039NB-M
• 00810034800855: 2039NB-S
• 00810034800848: 2039NB-XS