FDA UDI In Commercial Distribution 🇺🇸 United States

SR MCP

DI: 00886385021010 · Model: 5800-MD00 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SR MCP
Primary DI
00886385021010
Version / Model
5800-MD00
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-27
Public Version
4
Public Version Date
2022-05-13
Public Version Status
Update
Public Device Record Key
f74c24d8-87c0-4884-9250-f3da86f351c7

Device Description

SR MCP, IMPLANT, SIZE MEDIUM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MPK Semi-Constrained Metal/Polymer Finger Joint Prosthesis

GMDN Terms

Code Name
33786 Metacarpophalangeal joint prosthesis, one-piece

Identifiers

Type ID
Primary 00886385021010

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid exposure to direct sunlight or dampness