FDA UDI In Commercial Distribution 🇺🇸 United States

Ophtho-Burr®

DI: 00886158010012 · Model: 8550850 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ophtho-Burr®
Primary DI
00886158010012
Version / Model
8550850
Catalog Number
8550850
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
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
d7c8b7a5-3c72-4ab3-9814-abf1f79b5ae5

Device Description

OPHTHO-BURR DIAMOND BURR 2.5MM REUSABLE 1/EA

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HOG Burr, Corneal, Battery-Powered

GMDN Terms

Code Name
42443 Corneal bur system, battery-powered

Identifiers

Type ID
Primary 00886158010012

Customer Contacts

Phone
18669068080