FDA UDI In Commercial Distribution 🇺🇸 United States

Bausch + Lomb

DI: 00757770424740 · Model: E4800 · Bausch & Lomb Incorporated
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bausch + Lomb
Primary DI
00757770424740
Version / Model
E4800
Catalog Number
E4800
Company Name
Bausch & Lomb Incorporated
Labeler DUNS
196603781
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2019-10-07
Public Version Status
Update
Public Device Record Key
6d0e12bf-eb7d-4f82-bf04-152bb64f85c0

Device Description

HANDPIECE BACKFLUSH

Device Characteristics

Single Use
No
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
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HQC Unit, Phacofragmentation

GMDN Terms

Code Name
17899 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 00757770424740