TruAim Lapidus System Sterile, Single Use 991067S

GUDID 00857676008324

931

Eca Medical Instruments

Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use
Primary Device ID00857676008324
NIH Device Record Key80e66d7e-53c5-49c8-9a3e-fd06b3900b1e
Commercial Distribution StatusIn Commercial Distribution
Brand NameTruAim Lapidus System Sterile, Single Use
Version Model NumberA
Catalog Number991067S
Company DUNS084330422
Company NameEca Medical Instruments
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100857676008324 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-07-26
Device Publish Date2023-01-09

Devices Manufactured by Eca Medical Instruments

00857676008591 - Palm Handle, 2 mm Hex Torque Limiting Instrument2024-06-03
00857676008607 - Threaded Trimmable Fixation Nail H/W Instrument Pack2024-06-03
00857676008614 - Threaded Trimmable Fixation Nail F/A Instrument Pack2024-06-03
00857676008621 - Threaded Trimmable Fixation Nail Sizing Guide Pack2024-06-03
00857676008553 - iFUSE INTRA X Mallet2024-03-26
00857676008560 - iFUSE INTRA X Assist2024-03-26
00857676008577 - Orthopedic Cannulated Nail Instrument Pack 3.0 x 50mm2024-03-26
00857676008584 - Orthopedic Cannulated Nail Instrument Pack 4.0 x 100mm2024-03-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.