FDA UDI In Commercial Distribution 🇺🇸 United States

Intralasik Instruments

DI: 08175700112505 · Model: AS3-800 · AURORA SURGICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intralasik Instruments
Primary DI
08175700112505
Version / Model
AS3-800
Catalog Number
AS3-800
Company Name
AURORA SURGICAL, LLC
Labeler DUNS
968368832
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-23
Public Version
1
Public Version Date
2023-07-03
Public Version Status
New
Public Device Record Key
53f44305-7e7e-491e-b189-4fec204b628a

Device Description

Intralasik Flap Spatula Double Ended

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HND Spatula, Ophthalmic

GMDN Terms

Code Name
13120 Ophthalmic surgical probe, reusable

Identifiers

Type ID
Primary 08175700112505

Customer Contacts

Phone
7278213303