IntroDucer NRFit 001163-30L

GUDID 14048223028800

IntroDucer NRFit 1,0 x 30mm for the Standard SPROTTE® NRFit 22G

Pajunk GmbH Medizintechnologie

Nonimplantable needle guide, single-use

• Primary Device ID: 14048223028800
• NIH Device Record Key: 7087e751-d094-4c0b-b6a0-7dc37f44af1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IntroDucer NRFit
• Version Model Number: 001163-30L
• Catalog Number: 001163-30L
• Company DUNS: 317654283
• Company Name: Pajunk GmbH Medizintechnologie
• Device Count: 25
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	04048223028803 [Unit of Use]
GS1	14048223028800 [Primary]

FDA Product Code

• MDM: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

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: 2019-10-07
• Device Publish Date: 2018-06-12

On-Brand Devices [IntroDucer NRFit]

• 14048223033897: IntroDucer NRFit 1,0 x 40mm for the Standard SPROT
• 14048223028800: IntroDucer NRFit 1,0 x 30mm for the Standard SPROT
• 14048223028794: IntroDucer NRFit 0,8 x 30mm for the Standard SPROT
• 04048223132173: IntroDucer NRFit 1,0 x 40mm for the Standard SPROTTE® cannula 22G
• 04048223132166: IntroDucer NRFit 1,0 x 30mm for the Standard SPROTTE® NRFit 22G
• 04048223129784: IntroDucer NRFit 0,8 x 30mm for the Standard Sprotte Kanüle 24G/25G/26G/27G
• 04048223053867: IntroDucer NRFit 1,2 x 30mm for the Standard SPROTTE® NRFit 20G/21G