FDA UDI In Commercial Distribution 🇺🇸 United States

Diamatrix Ltd.

DI: 00813059018304 · Model: F942S · Diamatrix
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Diamatrix Ltd.
Primary DI
00813059018304
Version / Model
F942S
Catalog Number
F942S
Company Name
Diamatrix
Labeler DUNS
809555139
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-09
Public Version
1
Public Version Date
2022-06-17
Public Version Status
New
Public Device Record Key
68715282-6845-473c-b548-61336e5c52a3

Device Description

Buratto Lasik Flap Forceps, .8mm very delicate Disc-Shaped tip with serrated jaws, Vaulted Shafts, flat handle with hole pattern, 102mm total length, Stainless

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
HNR Forceps, Ophthalmic

GMDN Terms

Code Name
63413 Ophthalmic implant handling forceps, reusable

Identifiers

Type ID
Primary 00813059018304

Customer Contacts

Phone
2813678081