OptonPro 4682

GUDID 04053815053972

Zimmer MedizinSysteme GmbH

Musculoskeletal/physical therapy laser, professional
Primary Device ID04053815053972
NIH Device Record Key0aba112b-c8ab-44d6-8ced-2be534543be7
Commercial Distribution StatusIn Commercial Distribution
Brand NameOptonPro
Version Model Number4682
Catalog Number4682
Company DUNS316111251
Company NameZimmer MedizinSysteme GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com
Phone(800) 327-3576
Emailinfo@zimmerusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104053815053972 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-05-07
Device Publish Date2016-09-24

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