FDA UDI In Commercial Distribution 🇺🇸 United States

Dr. Fog® Treated Sponge

DI: 00840113206926 · Model: DF-3120 · ASPEN SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Dr. Fog® Treated Sponge
Primary DI
00840113206926
Version / Model
DF-3120
Company Name
ASPEN SURGICAL PRODUCTS, INC.
Labeler DUNS
027680821
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-25
Public Version
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
642583d2-e282-4c64-973c-5e48f1bc2834

Device Description

Intended to be used as an anti-fog agent for endoscopic camera lenses

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCT Anti fog solution and accessories, endoscopy

GMDN Terms

Code Name
45225 Endoscope antifog solution

Identifiers

Type ID
Package 00840113206957
Primary 00840113206926
Package 00840113206933

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K932449 000