FDA UDI In Commercial Distribution 🇺🇸 United States

AquaFlate

DI: 00850025153973 · Model: 251 · HR PHARMACEUTICALS INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AquaFlate
Primary DI
00850025153973
Version / Model
251
Company Name
HR PHARMACEUTICALS INC.
Labeler DUNS
828918164
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-20
Public Version
1
Public Version Date
2024-03-28
Public Version Status
New
Public Device Record Key
f9bfe6bc-5c1a-41c3-890f-bdd05a083fad

Device Description

AquaFlate 10mL Wide Pre-Filled Sterile Water Syringe

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
Yes
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
No

Product Codes

Code Name
EZL CATHETER, RETENTION TYPE, BALLOON

GMDN Terms

Code Name
44707 Device-irrigation sterile water

Identifiers

Type ID
Package 50850025153978
Primary 00850025153973

Customer Contacts

Phone
+1(717)252-1110 ext. 110