FDA UDI In Commercial Distribution 🇺🇸 United States

Bausch + Lomb

DI: 00757770418442 · Model: N5402 · Bausch & Lomb Incorporated
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bausch + Lomb
Primary DI
00757770418442
Version / Model
N5402
Catalog Number
N5402
Company Name
Bausch & Lomb Incorporated
Labeler DUNS
196603781
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-28
Public Version
1
Public Version Date
2025-08-05
Public Version Status
New
Public Device Record Key
98885402-19f6-41f0-9d9d-c089c3356313

Device Description

FORCEPS ADSON SERRATED

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
KAE Forceps, Ent

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 00757770418442