FDA UDI In Commercial Distribution 🇺🇸 United States

AQ-Flex™19

DI: 03760187910109 · Model: 211-0128 · MAUNA KEA TECHNOLOGIES
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AQ-Flex™19
Primary DI
03760187910109
Version / Model
211-0128
Catalog Number
MP-0010-AGF
Company Name
MAUNA KEA TECHNOLOGIES
Labeler DUNS
394136118
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a372abdf-f0a9-4668-9f27-762872d54355

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
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Hydrogen Peroxide

Product Codes

Code Name
OWN Confocal Optical Imaging

GMDN Terms

Code Name
62288 Confocal endomicroscopy system probe

Identifiers

Type ID
Primary 03760187910109

Customer Contacts

Phone
+33170080967