HALL MicroFree PRO8250SB

GUDID 10653405987512

Hall MicroFree Sagittal Saw XE

Conmed Corporation

Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable Bone/joint surgical power tool motorized handpiece/set, electric, reusable

• Primary Device ID: 10653405987512
• NIH Device Record Key: e9fea717-bc06-413d-aca1-541199628027
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HALL MicroFree
• Version Model Number: PRO8250SB
• Catalog Number: PRO8250SB
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	10653405987512 [Direct Marking]
GS1	20653405987519 [Primary]

FDA Product Code

• HAB: SAW, POWERED, AND ACCESSORIES

Sterilization

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

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

[10653405987512]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-07-25
• Device Publish Date: 2022-07-15

On-Brand Devices [HALL MicroFree]

• 30653405005753: HALL MicroFree Reciprocating Saw
• 30653405005746: HALL MicroFree Oscillating Saw
• 30653405005739: HALL MicroFree Sagittal Saw
• 30653405005722: HALL MicroFree Medium Speed Drill
• 30653405005715: HALL MicroFree High Speed Drill
• 10653405987512: Hall MicroFree Sagittal Saw XE