FDA UDI In Commercial Distribution 🇺🇸 United States

Beaver-Visitec

DI: 35055186236060 · Model: MMK110/3 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Beaver-Visitec
Primary DI
35055186236060
Version / Model
MMK110/3
Catalog Number
MMK110/3
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2021-11-15
Public Version
1
Public Version Date
2021-11-23
Public Version Status
New
Public Device Record Key
a535b9de-638b-448b-b422-b4895d9ff65d

Device Description

Malosa Core Suface Treatment Pack (20/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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PZG Surgical Eye Tray

GMDN Terms

Code Name
45150 Ophthalmic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Unit of Use 05055186236069
Primary 35055186236060