FDA UDI In Commercial Distribution 🇺🇸 United States

LMA

DI: 05060112311840 · Model: IPN900346 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LMA
Primary DI
05060112311840
Version / Model
IPN900346
Catalog Number
15230
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
2024-01-10
Public Version Status
Update
Public Device Record Key
7e1dfe0b-9737-4243-b24f-caa67b02f2c7

Device Description

LMA ProSeal Size 3 Pack

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
Yes
PM Exempt
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
CAE AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

GMDN Terms

Code Name
45036 Laryngeal mask airway, single-use

Identifiers

Type ID
Package 15060112311847
Primary 05060112311840

Customer Contacts