CitreLock Inserter Large 40-102-0002

GUDID 00810027270139

Acuitive Technologies, Inc.

Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable Surgical tamp, reusable

Primary Device ID	00810027270139
NIH Device Record Key	d334c8df-0934-40c0-83eb-36c5950a02b6
Commercial Distribution Status	In Commercial Distribution
Brand Name	CitreLock Inserter Large
Version Model Number	40-102-0002
Catalog Number	40-102-0002
Company DUNS	074645634
Company Name	Acuitive Technologies, Inc.
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	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	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx
Phone	201-661-2680
Email	xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810027270139 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K200725

FDA Product Code

HXG

Tamp