MEDICOM SAFETOUCH 1255HB

GUDID 20686864047364

MEDICOM SAFETOUCH DENTAL DAM 5 X 5 Inch

AMD Medicom Inc

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• Primary Device ID: 20686864047364
• NIH Device Record Key: d616d065-731d-47a6-a1e4-3ce684c3c626
• Commercial Distribution Discontinuation: 2024-02-06
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MEDICOM SAFETOUCH
• Version Model Number: 1255HB
• Catalog Number: 1255HB
• Company DUNS: 256880576
• Company Name: AMD Medicom Inc
• Device Count: 52
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca
• Phone: +1(514)636-6262
• Email: mkansou@medicom.ca

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place
• Special Storage Condition, Specify: Between 0 and 0 *Cool dry place

Device Identifiers

Device Issuing Agency	Device ID
GS1	00686864047360 [Unit of Use]
GS1	10686864047367 [Primary]
GS1	20686864047364 [Package]; Contains: 10686864047367; Package: Outer Case [6 Units]; Discontinued: 2024-02-06; Not in Commercial Distribution

FDA Product Code

• EIE: DAM, RUBBER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-07
• Device Publish Date: 2019-01-16

On-Brand Devices [MEDICOM SAFETOUCH]

• 20686864054720: MEDICOM SAFETOUCH DENTAL DAM
• 20686864054713: MEDICOM SAFETOUCH DENTAL DAM
• 00686864059592: Medicom SafeTouch EverStrong - Vinyl - Medical Examination Gloves - Powder-Free - Non-Sterile -
• 20686864014793: Medicom SafeTouch EverStrong - Vinyl - Medical Examination Gloves - Powder-Free - Non-Sterile -
• 20686864001557: Medicom SafeTouch EverStrong - Vinyl - Medical Examination Gloves - Powder-Free - Non-Sterile -
• 20686864001540: Medicom SafeTouch EverStrong - Vinyl - Medical Examination Gloves - Powder-Free - Non-Sterile -
• 20686864001526: Medicom SafeTouch EverStrong - Vinyl - Medical Examination Gloves - Powder-Free - Non-Sterile -
• 20686864047425: MEDICOM SAFETOUCH DENTAL DAM 6 X 6 Inch
• 20686864047395: MEDICOM SAFETOUCH DENTAL DAM 5 X 5 Inch
• 20686864047432: MEDICOM SAFETOUCH DENTAL DAM 6 X 6 Inch
• 20686864047371: MEDICOM SAFETOUCH DENTAL DAM 5 X 5 Inch
• 20686864047364: MEDICOM SAFETOUCH DENTAL DAM 5 X 5 Inch