FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD8031S0 · Model: SD8031s · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD8031S0
Version / Model
SD8031s
Catalog Number
SD8031s
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-02
Public Version
1
Public Version Date
2022-12-12
Public Version Status
New
Public Device Record Key
1cf3acc0-9a6b-40fb-9951-6533972dd3ed

Device Description

Mister Clear fog reduction, Sterile, Single use, 1 units, Sample

Device Characteristics

Single Use
Yes
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
No

Product Codes

Code Name
HET LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

GMDN Terms

Code Name
65462 Endoscope antifog sheath

Identifiers

Type ID
Primary B382SD8031S0

Customer Contacts