FDA UDI In Commercial Distribution 🇺🇸 United States

LMA

DI: 05060112311635 · Model: IPN046964 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
LMA
Primary DI
05060112311635
Version / Model
IPN046964
Catalog Number
178120
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-15
Public Version
3
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
4aee8f2a-8cec-4621-9001-b13082527812

Device Description

LMA Supreme® Airway Plus Pack Size 2

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
CAE AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

GMDN Terms

Code Name
45036 Laryngeal mask airway, single-use

Identifiers

Type ID
Package 15060112311632
Primary 05060112311635
Package 25060112311639

Customer Contacts