FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10888551002158 · Model: MICSO-605 · STERILMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10888551002158
Version / Model
MICSO-605
Catalog Number
SO-605
Company Name
STERILMED, INC.
Labeler DUNS
175899459
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-18
Public Version
3
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
41811c07-24f1-4013-a629-ce7a78cb3c97

Device Description

SAW BLADE SAGITTAL STRYKER SYSTEM 2000/4000 REPLACEMENT

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
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
61803 Surgical saw blade, sagittal, reprocessed

Identifiers

Type ID
Primary 10888551002158

Customer Contacts