FDA UDI In Commercial Distribution 🇺🇸 United States

Impactor – 10.75mm

DI: 00869826000379 · Model: 500627 · Si-Bone Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Impactor – 10.75mm
Primary DI
00869826000379
Version / Model
500627
Company Name
Si-Bone Inc.
Labeler DUNS
830127168
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
4213297d-6953-41c8-9665-012cf0e2f447

Device Description

Impactor – 10.75mm

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
58849 Sacroiliac joint transarticular fixation/arthrodesis implantation kit

Identifiers

Type ID
Primary 00869826000379

Customer Contacts

Phone
855-884-3873