FDA UDI In Commercial Distribution 🇺🇸 United States

Bausch + Lomb

DI: 10757770058461 · Model: BLP324MX30 · Bausch & Lomb Incorporated
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
Bausch + Lomb
Primary DI
10757770058461
Version / Model
BLP324MX30
Catalog Number
BLP324MX30
Company Name
Bausch & Lomb Incorporated
Labeler DUNS
196603781
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2016-11-08
Public Version
5
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
18a9e203-8ce5-4b82-a7cd-cec6f46b07a9

Device Description

2.2mm Sleeve and MICS Needle Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HQC Unit, Phacofragmentation

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 10757770058461
Unit of Use 20757770058468