FDA UDI In Commercial Distribution 🇺🇸 United States

Novaplus®

DI: 10809160022191 · Model: V300 · MEDICAL ACTION INDUSTRIES INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Novaplus®
Primary DI
10809160022191
Version / Model
V300
Company Name
MEDICAL ACTION INDUSTRIES INC.
Labeler DUNS
092364462
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-08-20
Public Version
3
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
c0c0fb9a-85db-4888-a5ab-097abb51d977

Device Description

Sponge: Lap 18X18 W 100/Cs

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
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
GDY GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Package 20809160022198
Primary 10809160022191
Unit of Use 40809160022192

Storage Conditions

Type
Special Storage Condition, Specify
Type
Special Storage Condition, Specify
Special Conditions
store at room temperature