FDA UDI Not in Commercial Distribution 🇺🇸 United States

Dr. Fog® Anti-fog Solution

DI: 00887761000032 · Model: DF-3100B · ASPEN SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Dr. Fog® Anti-fog Solution
Primary DI
00887761000032
Version / Model
DF-3100B
Company Name
ASPEN SURGICAL PRODUCTS, INC.
Labeler DUNS
027680821
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
7
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
91a9a333-63a7-4e97-8824-c0ced1044255
Distribution End Date
2022-07-07

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 20887761000036
Package 10887761000039
Primary 00887761000032

Customer Contacts