FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD922701030 · Model: SD92270103 · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD922701030
Version / Model
SD92270103
Catalog Number
SD92270103
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
2a9ea5e8-eabd-46ff-b71d-88dd92a6ad5b

Device Description

7 inch Kerrison Laminectomy Punch, 3mm Up

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
HTX RONGEUR

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary B382SD922701030

Customer Contacts