FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10810003223392 · Model: MK-800800-30 · MICROSPECIALITIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10810003223392
Version / Model
MK-800800-30
Catalog Number
MK-800800-30
Company Name
MICROSPECIALITIES, INC.
Labeler DUNS
013469890
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-31
Public Version
1
Public Version Date
2019-11-08
Public Version Status
New
Public Device Record Key
c67ebe27-162c-48ad-8eed-23f2aef8a706

Device Description

MicroKeratome Blades, Laser Calibrated NIDEK minus 30. Have the ultimate control of corneal flap thickness while using a single head. Range from -40 to +20 microns. 10/bx

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HNO Keratome, Ac-Powered

GMDN Terms

Code Name
44722 Keratome blade, single-use

Identifiers

Type ID
Package 30810003223396
Primary 10810003223392

Customer Contacts

Phone
203-874-1832

Device Sizes

Type Value Unit Text
Angle -30 degree