Jenker A87013

GUDID D003A870131

Jenker Needle Recapper

Dentsply Professional

Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable Needle recapping device, reusable

• Primary Device ID: D003A870131
• NIH Device Record Key: 79c97ce1-4b40-4323-9eb9-57f1e3facf0e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jenker
• Version Model Number: A87013
• Catalog Number: A87013
• Company DUNS: 144140845
• Company Name: Dentsply Professional
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.
• Special Storage Condition, Specify: Between 0 and 0 *Read Instructions for Use
• Special Storage Condition, Specify: Between 0 and 0 *Recapping step must be carried out one-handed to prevent the possibility of needle sticks.

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D003A870131 [Primary]

FDA Product Code

• DZM: NEEDLE, DENTAL

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: 2022-12-05
• Device Publish Date: 2022-11-26

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