FDA UDI In Commercial Distribution 🇺🇸 United States

Visitec®

DI: 30886158010129 · Model: 8590300 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Visitec®
Primary DI
30886158010129
Version / Model
8590300
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-01-19
Public Version
1
Public Version Date
2022-01-27
Public Version Status
New
Public Device Record Key
19b67193-b03f-435a-ab89-99c0f78c5a5e

Device Description

EYE BANDAGE GUIBOR BUBBLE BANDAGE STERILE 10/BX

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

GMDN Terms

Code Name
42443 Corneal bur system, battery-powered

Identifiers

Type ID
Unit of Use 00886158010128
Primary 30886158010129

Customer Contacts

Phone
18669068080