FDA UDI In Commercial Distribution 🇺🇸 United States

Aura40

DI: 05707480037636 · Model: 326150000U · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Aura40
Primary DI
05707480037636
Version / Model
326150000U
Catalog Number
326150000U
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-02
Public Version
1
Public Version Date
2023-03-10
Public Version Status
New
Public Device Record Key
303c35b2-8639-45a4-a610-38a663a35066

Device Description

Ambu Aura40 U Size 1.5

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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
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 05707480037629
Primary 05707480037636

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Device Size Text, specify 1,5