FDA UDI In Commercial Distribution 🇺🇸 United States

Bausch + Lomb

DI: 00757770433353 · Model: N5941 10 · Bausch & Lomb Incorporated
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bausch + Lomb
Primary DI
00757770433353
Version / Model
N5941 10
Catalog Number
N5941 10
Company Name
Bausch & Lomb Incorporated
Labeler DUNS
196603781
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
252ef11f-75de-4b17-a258-06a31ac9b8b5

Device Description

SILICONE TUBE .104"x.192"x10FT

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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
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
GBX Catheter, Irrigation

GMDN Terms

Code Name
10217 Surgical suction system

Identifiers

Type ID
Primary 00757770433353