7210498

GUDID 00885556539682

MTOLAPAROSCOPE 5.5 X O DEG X 170 WL

Smith & Nephew, Inc.

Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope Rigid optical laparoscope
Primary Device ID00885556539682
NIH Device Record Key4ac790e5-c035-472e-9ea5-ef9cb0117bcd
Commercial Distribution Discontinuation2017-04-03
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number7210498
Catalog Number7210498
Company DUNS109903521
Company NameSmith & Nephew, 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 Usefalse
Lot Batchfalse
Serial Numbertrue
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(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100885556539682 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


[00885556539682]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-30

Devices Manufactured by Smith & Nephew, Inc.

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00885556890745 - Q-FIX2024-05-06 Q-FIX ULTRA
00885556890752 - ULTRABRACE2024-05-06 ULTRABRACE KIT
00885556890769 - FOOTPRINT2024-05-06 FOOTPRINT MINI PK 3.5MM
00885556890790 - Q-FIX2024-05-06 2.9MM CANNULATED DRILL FOR Q-FIX ULTRA & 1.25MM DRILL PIN
00885556890912 - FOOTPRINT2024-05-06 FOOTPRINT MINI DRILL 3.5MM
00885556901335 - FOOTPRINT2024-05-06 FOOTPRINT MINI DRILL 3.7MM
20885556817692 - TULA2024-05-06 TULA EARPLUG 10-PACK- SIZE 2 (NST007071)

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