UNIVERSAL SCREW REMOVAL SYSTEM

GUDID 00888118113962

KLS-Martin L.P.

Surgical screwdriver, reusable
Primary Device ID00888118113962
NIH Device Record Keyb773943c-d45a-40a6-b26a-6f2a5ae2100e
Commercial Distribution StatusIn Commercial Distribution
Brand NameUNIVERSAL SCREW REMOVAL SYSTEM
Version Model Number99-592-10-02
Company DUNS826499238
Company NameKLS-Martin L.P.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100888118113962 [Primary]

FDA Product Code

HXXSCREWDRIVER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888118113962]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-20
Device Publish Date2018-09-26

On-Brand Devices [UNIVERSAL SCREW REMOVAL SYSTEM]

0088811811396299-592-10-02
0088811811395599-592-10-01
0088811807671750-425-27-07
0088811807670050-425-26-07
0088811807669450-425-25-07
0088811807668750-425-24-07
0088811807667050-425-23-07
0088811807666350-425-22-07
0088811807665650-425-21-07
0088811807664950-425-20-07
0088811807663250-425-19-07
0088811807662550-425-18-07
0088811807661850-425-17-07
0088811807660150-425-16-07
0088811807659550-425-15-07
0088811807658850-425-14-07
0088811807657150-425-13-07
0088811807656450-425-12-07
0088811807655750-425-11-07
0088811808804855-964-32-04
0088811808803155-964-31-04
0088811808747855-963-29-04
0088811807738750-610-00-04
0088811807737050-600-00-04

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