SMI7206011

GUDID 10888551034364

SHAVER BLADE BONECUTTER FULL RADIUS YELLOW/BLACK

STERILMED, INC.

Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed
Primary Device ID10888551034364
NIH Device Record Key27d219a2-17c9-42c2-8e2a-4dbef91bb1dc
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberSMI7206011
Catalog NumberSMI7206011
Company DUNS175899459
Company NameSTERILMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com
Phone+1(888)541-0078
Emailsterilmedcs@its.jnj.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110888551034364 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXARTHROSCOPE

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

[10888551034364]

Ethylene Oxide

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-22

Devices Manufactured by STERILMED, INC.

10888551045179 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
10888551045186 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
10888551045193 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
10888551045209 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
10888551010313 - NA2021-01-22 KNIFE SET ECTRA II (PACK OF 3)
10888551021531 - NA2021-01-22 KNIVES (1) HOOK BLADE (1) TRIANGLE BLADE ENDOTRAC BLADE SYSTEM
10888551000048 - NA2020-11-06 CTS RELIEF KIT, 5PC SET
10888551012928 - NA2020-10-19 ENDO LUNG
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.