Dummy, silver, type COD AGD.A30

GUDID 04049223104870

Eckert & Ziegler BEBIG GmbH

Manual brachytherapy source, temporary placement
Primary Device ID04049223104870
NIH Device Record Key02d7e2e3-4020-429a-8670-60a83d9a7f0c
Commercial Distribution StatusIn Commercial Distribution
Brand NameDummy, silver, type COD
Version Model NumberAGD.A30
Catalog NumberAGD.A30
Company DUNS331080432
Company NameEckert & Ziegler BEBIG GmbH
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
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

Phone+4930941084130
Emailinfo@bebig.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a clean, dry environment (relative humidity < 95%). Make sure that the packaging is not damaged, and that no chemicals are in close proximity to the storage location.

Device Identifiers

Device Issuing AgencyDevice ID
GS104049223104870 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KXKSource, Brachytherapy, Radionuclide

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04049223104870]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-24

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