FDA UDI In Commercial Distribution 🇺🇸 United States

Visitec®

DI: 30886158102435 · Model: 585233 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

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Basic Information

Brand Name
Visitec®
Primary DI
30886158102435
Version / Model
585233
Catalog Number
585233
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-12-21
Public Version
1
Public Version Date
2021-12-29
Public Version Status
New
Public Device Record Key
a923146b-4180-43f0-946f-dba148a16146

Device Description

LASIK Flap Roller [Lindstrom] 14mm

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
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
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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
46705 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Identifiers

Type ID
Unit of Use 00886158102434
Primary 30886158102435

Customer Contacts

Phone
18669068080