PEROUSE MEDICAL VPEE63101DL

GUDID 33661234025184

NEEDLE GUIDE Ø0,9MM

PEROUSE MEDICAL

Needle guide, single-use

• Primary Device ID: 33661234025184
• NIH Device Record Key: 59c6da2c-90c8-4ecc-9783-cfbbd826d6df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PEROUSE MEDICAL
• Version Model Number: E63101DL
• Catalog Number: VPEE63101DL
• Company DUNS: 267476323
• Company Name: PEROUSE MEDICAL
• Device Count: 2
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03661234025183 [Primary]
GS1	33661234025184 [Package]; Contains: 43661234025181; Package: [1 Units]; In Commercial Distribution
GS1	43661234025181 [Package]; Contains: 03661234025183; Package: [5 Units]; In Commercial Distribution
GS1	63661234025185 [Unit of Use]

FDA Product Code

• GDF: GUIDE, NEEDLE, SURGICAL

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: 2024-03-28
• Device Publish Date: 2024-03-20

On-Brand Devices [PEROUSE MEDICAL]

• 33661234025269: NEEDLE GUIDE Ø2,25MM
• 33661234025252: NEEDLE GUIDE Ø1,2MM
• 33661234025245: NEEDLE GUIDE Ø1,0MM
• 43661234025228: NEEDLE GUIDE Ø1,8MM
• 33661234025184: NEEDLE GUIDE Ø0,9MM
• 43661234025235: NEEDLE GUIDE Ø0,9MM
• 43661234025198: NEEDLE GUIDE Ø1,0MM
• 33661234025207: NEEDLE GUIDE Ø1,2MM
• 33661234025214: NEEDLE GUIDE Ø1,4MM