FDA UDI In Commercial Distribution 🇺🇸 United States

Visitec®

DI: 30886158102183 · Model: 585189 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Visitec®
Primary DI
30886158102183
Version / Model
585189
Catalog Number
585189
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-06
Public Version
1
Public Version Date
2024-06-14
Public Version Status
New
Public Device Record Key
7e31b5e2-c396-480c-8c66-3fa094c8e867

Device Description

SPATULA EXCIMER (5/SP)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HND Spatula, ophthalmic

GMDN Terms

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

Identifiers

Type ID
Primary 30886158102183

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place.