CFM Technologies CM2-BK

GUDID 00850013958085

Cerumen Management Set with reusable and single-use curettes.

C F M TECHNOLOGIES INC

Endaural curette, single-use
Primary Device ID00850013958085
NIH Device Record Key3b26e5ed-6fae-4cc8-893a-13aec52781dc
Commercial Distribution StatusIn Commercial Distribution
Brand NameCFM Technologies
Version Model NumberCM2 black
Catalog NumberCM2-BK
Company DUNS040748944
Company NameC F M TECHNOLOGIES INC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com
Phone6039243751
Emailcfm@cfmtechnologies.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850013958085 [Primary]

FDA Product Code

JYGCurette, Ear

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-14
Device Publish Date2020-01-06

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00850013958115Cerumen Management Set with single-use curettes.
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