CELEROMARK CELEROMARK

GUDID 05420045503376

Hologic, Inc.

Imaging lesion localization marker, implantable

• Primary Device ID: 05420045503376
• NIH Device Record Key: 0dbe8fcd-8b3f-4f91-8468-ae5dceae9332
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CELEROMARK
• Version Model Number: CELEROMARK
• Catalog Number: CELEROMARK
• Company DUNS: 018925968
• Company Name: Hologic, Inc.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05420045503376 [Primary]
GS1	15420045503373 [Package]; Package: BOX [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K023450

FDA Product Code

• NEU: MARKER, RADIOGRAPHIC, IMPLANTABLE

Sterilization

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

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

[05420045503376]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-04

On-Brand Devices [CELEROMARK]

• 05420045503383: CELEROMARK-2S
• 05420045503376: CELEROMARK