FDA UDI In Commercial Distribution 🇺🇸 United States

MORIA

DI: 03700483608195 · Model: CBM / ALTK HEAD 200 · MORIA SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MORIA
Primary DI
03700483608195
Version / Model
CBM / ALTK HEAD 200
Catalog Number
19170/200
Company Name
MORIA SA
Labeler DUNS
275937506
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-03
Public Version
1
Public Version Date
2024-05-13
Public Version Status
New
Public Device Record Key
5a6a16ff-563d-445a-a183-353b7982a5a7

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HMY Keratome, Battery-Powered

GMDN Terms

Code Name
62703 Microkeratome

Identifiers

Type ID
Primary 03700483608195