Jenker A87013

GUDID D003A870131

Jenker Needle Recapper

Dentsply Professional

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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