Silicone MCP TRL-500-50

GUDID 00885556857137

SMCP TRIAL SZ 50

Smith & Nephew, Inc.

Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable
Primary Device ID00885556857137
NIH Device Record Keyb6b01133-02a6-4e02-a63c-b56ba4eeb67c
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilicone MCP
Version Model NumberTRL-500-50
Catalog NumberTRL-500-50
Company DUNS045483575
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100885556857137 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KYJProsthesis, finger, constrained, polymer

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


[00885556857137]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-09-07
Device Publish Date2022-12-22

On-Brand Devices [Silicone MCP]

00885556857137SMCP TRIAL SZ 50
00885556857120SMCP TRIAL SZ 40
00885556857113SMCP TRIAL SZ 30
00885556857106SMCP TRIAL SZ 20
00885556857090SMCP TRIAL SZ 10
00885556857083SMCP TRIAL SZ. 05
00885556856925SILICONE MCP SZ 50
00885556856918SILICONE MCP SZ 40
00885556856901SILICONE MCP SZ 30
00885556856895SILICONE MCP SZ 20
00885556856888SILICONE MCP SZ 10
00885556856871SILICONE MCP SZ 05

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