FDA UDI In Commercial Distribution 🇺🇸 United States

LASIK Shield

DI: 00813465011302 · Model: 7302 · HURRICANE MEDICAL INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

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Basic Information

Brand Name
LASIK Shield
Primary DI
00813465011302
Version / Model
7302
Catalog Number
7302
Company Name
HURRICANE MEDICAL INC
Labeler DUNS
093377724
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-04-26
Public Version
5
Public Version Date
2020-04-14
Public Version Status
Update
Public Device Record Key
01caa0ff-1171-46a1-a2ee-4dceaacf8130

Device Description

The LASIK shield is used to protect and moisten the corneal flap during 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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization, Ethylene Oxide

Product Codes

Code Name
HOZ Sponge, Ophthalmic

GMDN Terms

Code Name
13704 Ophthalmic sponge

Identifiers

Type ID
Primary 00813465011302
Unit of Use 10813465011309

Customer Contacts

Phone
9417510588

Premarket Submissions

Submission Number Supplement Number
K990671 000

Device Sizes

Type Value Unit Text
Outer Diameter 8 Millimeter