FDA UDI In Commercial Distribution 🇺🇸 United States

BL Registration Tube - Broach

DI: 00810055525614 · Model: 503094 · Si-Bone Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BL Registration Tube - Broach
Primary DI
00810055525614
Version / Model
503094
Company Name
Si-Bone Inc.
Labeler DUNS
830127168
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-20
Public Version
1
Public Version Date
2025-10-28
Public Version Status
New
Public Device Record Key
99949556-434b-45e2-b69d-19c35a032700

Device Description

BL Registration Tube - Broach

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
Yes
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 00810055525614

Customer Contacts

Phone
855-884-3873