Primary Device ID | 00886385025308 |
NIH Device Record Key | 95362513-01f8-48cd-b2a4-4515fdd2c59f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SILICONE MCPX |
Version Model Number | MCPX-005 |
Catalog Number | MCPX-005 |
Company DUNS | 481999654 |
Company Name | Stryker Trauma SA |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886385025308 [Primary] |
KYJ | PROSTHESIS, FINGER, CONSTRAINED, POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00886385025308]
Moist Heat or Steam Sterilization
[00886385025308]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-09-24 |
Device Publish Date | 2016-09-24 |
00886385025421 | PreFlex MCP Sizer, Size 60 |
00886385025407 | PreFlex MCP Sizer, Size 50 |
00886385025384 | PreFlex MCP Sizer, Size 40 |
00886385025360 | PreFlex MCP Sizer, Size 30 |
00886385025346 | PreFlex MCP Sizer, Size 20 |
00886385025322 | PreFlex MCP Sizer, Size 10 |
00886385025308 | PreFlex MCP Sizer, Size 00 |
00886385025209 | Instrument Tray Lid |