FDA UDI In Commercial Distribution 🇺🇸 United States

23G SERRATED FORCEPS 128

DI: 04058935005405 · Model: SUI11-12 · Bausch & Lomb GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

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Basic Information

Brand Name
23G SERRATED FORCEPS 128
Primary DI
04058935005405
Version / Model
SUI11-12
Catalog Number
SUI11-12
Company Name
Bausch & Lomb GmbH
Labeler DUNS
344609518
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2023-09-12
Public Version
3
Public Version Date
2025-04-04
Public Version Status
Update
Public Device Record Key
c7876921-13dd-4c79-b73b-bc53fd76ba16

Device Description

Single Use Medical Device for Ophthalmic Surgery

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HNR Forceps, Ophthalmic

GMDN Terms

Code Name
62478 Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

Identifiers

Type ID
Unit of Use 24058935005409
Primary 04058935005405