FDA UDI In Commercial Distribution 🇺🇸 United States

Cygnus

DI: 20840113299212 · Model: WN0909-2 · ASPEN SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

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Basic Information

Brand Name
Cygnus
Primary DI
20840113299212
Version / Model
WN0909-2
Catalog Number
WN0909-2
Company Name
ASPEN SURGICAL PRODUCTS, INC.
Labeler DUNS
027680821
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2026-04-13
Public Version
1
Public Version Date
2026-04-21
Public Version Status
New
Public Device Record Key
be5c114e-0690-4f06-9c8d-4a17c7ae0e08

Device Description

CLEAR PATH LINT-FREE, ABSORBENT, NON-STERILE WIPERS,2 WIPERS PER BAG,100 BAGS PER CASE, 200 WIPERS TOTAL.POLYESTER, LATEX-FREE & SINGLE USE - SIZE 9"X9"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FRL Fiber, Medical, Absorbent

GMDN Terms

Code Name
66033 Endoscopic device drying tubing

Identifiers

Type ID
Unit of Use 00840113299218
Primary 20840113299212