FDA UDI In Commercial Distribution 🇺🇸 United States

Kittner

DI: 20749915000722 · Model: 45-01 · AMERICAN SURGICAL COMPANY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
Kittner
Primary DI
20749915000722
Version / Model
45-01
Company Name
AMERICAN SURGICAL COMPANY, LLC
Labeler DUNS
151054954
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2016-06-30
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
427f5d75-703b-4c27-be25-3433e9af40ce

Device Description

Cotton Kittner 9/16" x 1/4"

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EFQ Gauze/Sponge, Internal

GMDN Terms

Code Name
13698 Dissection sponge

Identifiers

Type ID
Primary 20749915000722
Unit of Use 10749915000725

Premarket Submissions

Submission Number Supplement Number
K872808 000