FDA UDI In Commercial Distribution 🇺🇸 United States

Ultracell

DI: 30886158015032 · Model: NSNETSTRIP19 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
500

Basic Information

Brand Name
Ultracell
Primary DI
30886158015032
Version / Model
NSNETSTRIP19
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2021-10-06
Public Version Status
Update
Public Device Record Key
db4563b0-052e-4074-baee-cd0cf967f71f

Device Description

PVA Strip 19mm Width

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
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EMX BALLOON, EPISTAXIS

GMDN Terms

Code Name
13704 Ophthalmic sponge

Identifiers

Type ID
Primary 30886158015032
Unit of Use 00886158015031

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place.