Smart kit Pro

GUDID 08800080201029

BSL

Autologous adipose tissue collection/injection set
Primary Device ID08800080201029
NIH Device Record Key4769e1f5-93ca-4f2a-935c-611a09681861
Commercial Distribution StatusIn Commercial Distribution
Brand NameSmart kit Pro
Version Model NumberSKT-24060
Company DUNS694860273
Company NameBSL
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com
Phone+82553289235
Emailbsl@biosl.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108800080201029 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QKLLipoaspirate Washing System For Aesthetic Body Contouring

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-19
Device Publish Date2023-05-11

On-Brand Devices [Smart kit Pro]

08800080201067SKT-22460
08800080201050SKT-12460
08800080201043SKT-22440
08800080201036SKT-12440
08800080201029SKT-24060
08800080201012SKT-14060

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