FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD1204740 · Model: SD1-20474 · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD1204740
Version / Model
SD1-20474
Catalog Number
SD1-20474
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-23
Public Version
1
Public Version Date
2022-12-01
Public Version Status
New
Public Device Record Key
a0f8e2fb-2215-4d4b-b712-31c7ee0a66ee

Device Description

Wide Punch Low Profile Stright Jaw, Sheath Curved Right 12° Medium, 1.9mm Tip-Profile 3.2mm Bite, 5.

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
35541 Spinal rongeur

Identifiers

Type ID
Primary B382SD1204740

Customer Contacts