FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD9144040780 · Model: SD914404078 · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD9144040780
Version / Model
SD914404078
Catalog Number
SD914404078
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-10
Public Version
1
Public Version Date
2025-07-18
Public Version Status
New
Public Device Record Key
e1247958-a05d-4955-b49f-d5c542697209

Device Description

5 1/2" Hoke Osteotome, Straight, 3mm Blade

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KDG CHISEL (OSTEOTOME)

GMDN Terms

Code Name
12844 Orthopaedic osteotome

Identifiers

Type ID
Primary B382SD9144040780

Customer Contacts