FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD5080310 · Model: SD50-8031 · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD5080310
Version / Model
SD50-8031
Catalog Number
SD50-8031
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-03
Public Version
1
Public Version Date
2022-12-12
Public Version Status
New
Public Device Record Key
f172947c-a4dc-45a4-8f9e-f7bf51e58a4a

Device Description

Latex Free 10 ft Insufflation Tubing, Luer Lock w/.1 Micron Filter and Mister Clear Fog Reduction Pack

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
NBH Accessories, arthroscopic

GMDN Terms

Code Name
35048 Bone lever/elevator, reusable

Identifiers

Type ID
Primary B382SD5080310

Customer Contacts