SILICONE MCPX MCPX-605

GUDID 00886385025421

Surgical implant template, reusable Surgical implant template, reusable

Primary Device ID	00886385025421
NIH Device Record Key	4f48a0c8-0567-4096-a4c8-15fde9abd7a8
Commercial Distribution Status	In Commercial Distribution
Brand Name	SILICONE MCPX
Version Model Number	MCPX-605
Catalog Number	MCPX-605
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	00886385025421 [Primary]

KYJ	PROSTHESIS, FINGER, CONSTRAINED, POLYMER

Steralize Prior To Use	true
Device Is Sterile	false

[00886385025421]

Moist Heat or Steam Sterilization

[00886385025421]

Moist Heat or Steam Sterilization