FDA UDI In Commercial Distribution 🇺🇸 United States

LMA

DI: 14026704743497 · Model: IPN924708 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LMA
Primary DI
14026704743497
Version / Model
IPN924708
Catalog Number
MVAXL2Y-CPNB
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-14
Public Version
2
Public Version Date
2023-10-27
Public Version Status
Update
Public Device Record Key
2fbf5f05-cb73-4b25-8063-a85b156d54ae

Device Description

ARROW AutoFuser Disposable Pain Control Pump

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MEB Pump, infusion, elastomeric

GMDN Terms

Code Name
47190 Elastomeric infusion pump kit

Identifiers

Type ID
Package 24026704743494
Primary 14026704743497

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090300 000