SPIDER 72204734

GUDID 00885556537411

SPIDER RE-PACK KIT

Smith & Nephew, Inc.

Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner Leg procedure positioner
Primary Device ID00885556537411
NIH Device Record Key744aa2b3-41e7-4ee1-8427-224f85c3ae34
Commercial Distribution StatusIn Commercial Distribution
Brand NameSPIDER
Version Model Number72204734
Catalog Number72204734
Company DUNS109903521
Company NameSmith & Nephew, Inc.
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 Usetrue
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(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
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
GS100885556537411 [Primary]

FDA Product Code

FWZAccessories, operating-room, table (kit)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-11-08
Device Publish Date2016-04-12

On-Brand Devices [SPIDER]

00885556570692RFB ACCESSORY TRACTION
00885556537442SPIDER CONNECTING HOSE KIT
00885556537435SPIDER INLET HOSE KIT
00885556537411SPIDER RE-PACK KIT
00885554032185SPIDER2 SHOULDER STABILIZATION KIT
00885554023534SPIDER 2 TENET 7615
008855540234803D SPIDER CONNECTOR TENET 7625
00885554023459SPIDER LEG ACCESSORY (RIGHT) TENET 7626
20885554018282SPIDER ANKLE STABILIZATION KITS
23596010511236KIT STABILIZATION SHOULDER (12)
00885556533253SPIDER2 ELECTRIC FOOT PEDAL REPLACEMENT

Trademark Results [SPIDER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SPIDER
SPIDER
97876272 not registered Live/Pending
Smith & Nephew, Inc.
2023-04-06
SPIDER
SPIDER
97739555 not registered Live/Pending
Sev1Tech, LLC
2023-01-03
SPIDER
SPIDER
97382480 not registered Live/Pending
Alfi International, Inc.
2022-04-26
SPIDER
SPIDER
97114275 not registered Live/Pending
MacSports, Inc.
2021-11-08
SPIDER
SPIDER
97044036 not registered Live/Pending
Terra Sonic International, LLC
2021-09-24
SPIDER
SPIDER
90767537 not registered Live/Pending
Geocent, LLC
2021-06-10
SPIDER
SPIDER
90734444 not registered Live/Pending
Interactive Education Concepts, Inc.
2021-05-25
SPIDER
SPIDER
90402817 not registered Live/Pending
Dakota Plumbing Products, LLC
2020-12-22
SPIDER
SPIDER
90358699 not registered Live/Pending
Robaina Direct LLC
2020-12-04
SPIDER
SPIDER
90314598 not registered Live/Pending
Springfield, Inc.
2020-11-12
SPIDER
SPIDER
90058757 not registered Live/Pending
SAFRAN TEST CELLS, INC.
2020-07-17
SPIDER
SPIDER
90022425 not registered Live/Pending
Cues, Inc.
2020-06-26

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