ETHICON PCP40

GUDID 20705031047829

Polymer Pledget PTFE Suture Butress

Johnson & Johnson International Inc.

Suture retention device

• Primary Device ID: 20705031047829
• NIH Device Record Key: b66a3d23-7d01-431f-a685-aa99cb3f4067
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ETHICON
• Version Model Number: PCP40
• Catalog Number: PCP40
• Company DUNS: 372587696
• Company Name: Johnson & Johnson International Inc.
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705031047822 [Primary]
GS1	20705031047829 [Package]; Contains: 10705031047822; Package: BOX [36 Units]; In Commercial Distribution

FDA Product Code

• DXZ: PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-07-24
• Device Publish Date: 2015-09-01

On-Brand Devices [ETHICON]

• 20705031047836: Polymer Pledget PTFE Suture Butress
• 20705031047829: Polymer Pledget PTFE Suture Butress
• 20705031047812: Polymer Pledget PTFE Suture Butress