FDA UDI In Commercial Distribution 🇺🇸 United States

Lamira

DI: 00744229678465 · Model: 678G1040 · PARI RESPIRATORY EQUIPMENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Lamira
Primary DI
00744229678465
Version / Model
678G1040
Company Name
PARI RESPIRATORY EQUIPMENT, INC.
Labeler DUNS
804736098
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-08
Public Version
1
Public Version Date
2019-02-08
Public Version Status
New
Public Device Record Key
0df57c90-b1f8-46fb-8d7a-68f26f037cf8

Device Description

Lamira Nebulizer System

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAF Nebulizer (Direct Patient Interface)

GMDN Terms

Code Name
12719 Ultrasonic nebulizing system

Identifiers

Type ID
Package 00744229100676
Primary 00744229678465