FDA UDI In Commercial Distribution 🇺🇸 United States

Reprocessed Sagittal Saw Blade

DI: B390AR300041S1 · Model: AR-300-041S · SURETEK MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reprocessed Sagittal Saw Blade
Primary DI
B390AR300041S1
Version / Model
AR-300-041S
Company Name
SURETEK MEDICAL
Labeler DUNS
785616934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-16
Public Version
2
Public Version Date
2024-02-23
Public Version Status
Update
Public Device Record Key
a3c66213-20d2-431a-8848-9b5d45b8d84a

Device Description

300 Sagittal Saw Blade, 40 x 9.5 x 0.6mm

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
No

Product Codes

Code Name
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

GMDN Terms

Code Name
61803 Surgical saw blade, sagittal, reprocessed

Identifiers

Type ID
Primary B390AR300041S1