FDA UDI In Commercial Distribution 🇺🇸 United States

Visitec®

DI: 30886158102657 · Model: 585742 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Visitec®
Primary DI
30886158102657
Version / Model
585742
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
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
0d5d2979-9a46-426d-86b2-19a27db1c0df

Device Description

BULK CANN ANTERIOR CHAMBER 1.6MM (100/SP)

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
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
46705 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Identifiers

Type ID
Primary 30886158102657
Unit of Use 00886158102656

Customer Contacts

Phone
18669068080