LiNA Skin Hook™ SH-110

GUDID 05708265000814

SMALL SHARP, dual pack

Lina Medical ApS

Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use Surgical retractor/retraction system blade, single-use
Primary Device ID05708265000814
NIH Device Record Key4d418d77-fbb0-46f2-9efb-9c1abb4763bb
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiNA Skin Hook™
Version Model NumberSH-110
Catalog NumberSH-110
Company DUNS305088619
Company NameLina Medical ApS
Device Count2
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
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+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com
Phone+48 612222142
Emailinfo.poland@lina-medical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100000000000000 [Unit of Use]
GS105708265000401 [Primary]
GS105708265000814 [Package]
Contains: 05708265000401
Package: box [5 Units]
In Commercial Distribution
GS105708265012657 [Unit of Use]

FDA Product Code

GADRetractor

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-04-23
Device Publish Date2016-09-23

On-Brand Devices [LiNA Skin Hook™]

05708265000838LARGE BLUNT, dual pack
05708265000821SMALL BLUNT, dual pack
05708265000814SMALL SHARP, dual pack

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