FDA UDI In Commercial Distribution 🇺🇸 United States

AQUILAVIE

DI: 10810118890229 · Model: J10452 · Ahc Americas LLC
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
AQUILAVIE
Primary DI
10810118890229
Version / Model
J10452
Catalog Number
J10452
Company Name
Ahc Americas LLC
Labeler DUNS
118840015
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-04-27
Public Version
1
Public Version Date
2023-05-05
Public Version Status
New
Public Device Record Key
97d61ec9-4235-4ef5-8d3d-13be2040a3e6

Device Description

Sterile Hypodermic Syringes for Single Use, 20mL, 50pcs/box, 12boxes/carton

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
MEG Syringe, Antistick
FMF Syringe, Piston
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
35904 Metered-delivery hypodermic syringe

Identifiers

Type ID
Unit of Use 00810118890222
Primary 10810118890229
Package 20810118890226