Applicator Brachytherapy Kit APPKITI125

GUDID 00815165020707

Eckert & Ziegler Bebig, Inc.

Manual brachytherapy system Manual brachytherapy system
Primary Device ID00815165020707
NIH Device Record Key4d377259-4301-40eb-854f-42d4918bb719
Commercial Distribution StatusIn Commercial Distribution
Brand NameApplicator Brachytherapy Kit
Version Model NumberApplicator Brachytherapy Kit I125
Catalog NumberAPPKITI125
Company DUNS021125001
Company NameEckert & Ziegler Bebig, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone203-262-0571
Emailned.lanfranco@bebig.com
Phone203-262-0571
Emailned.lanfranco@bebig.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100815165020707 [Primary]

FDA Product Code

IWJSystem, Applicator, Radionuclide, Manual

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-10-27

On-Brand Devices [Applicator Brachytherapy Kit]

00815165020745Applicator Brachytherapy Kit PD103
00815165020707Applicator Brachytherapy Kit I125
00081516502073Applicator Brachytherapy Kit PD103
00081516502072Applicator Brachytherapy Kit I125
00815165020721Applicator Brachytherapy Kit I125

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