AUT179075P

GUDID 10888551013109

BLUNTPORT PLUS CONVERTERLESS W/BLUNTGRIP THREADED ANCHOR

STERILMED, INC.

Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed Laparoscopic trocar blade, reprocessed
Primary Device ID10888551013109
NIH Device Record Key71521488-bd01-4d0b-bd78-c2a9fb47c456
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberAUT179075P
Catalog NumberAUT179075P
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110888551013109 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NLMLAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

[10888551013109]

Ethylene Oxide

Device Entry Metadata

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

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10888551045209 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
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