FDA UDI In Commercial Distribution 🇺🇸 United States

Autoject EI

DI: 00384701310010 · Model: AJ1310 · OWEN MUMFORD LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Autoject EI
Primary DI
00384701310010
Version / Model
AJ1310
Catalog Number
AJ1310
Company Name
OWEN MUMFORD LIMITED
Labeler DUNS
217266915
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
eb1114d8-ac6a-4e80-87cd-b2715e244a4d

Device Description

Non-sterile reusable autoinjector device, with an external indicator, for the injection of FDA-approved drugs from fixed needle syringes

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KZH Introducer, Syringe Needle

GMDN Terms

Code Name
12132 Syringe-loaded medication/vaccine injector, manual, professional

Identifiers

Type ID
Primary 00384701310010
Package 00384701310034

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K945660 000

Device Sizes

Type Value Unit Text
Width 25 Millimeter
Length 210 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius