FDA UDI In Commercial Distribution 🇺🇸 United States

Ambu® SPUR® II Adult Resuscitator

DI: 05707480153671 · Model: 520611000E · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Ambu® SPUR® II Adult Resuscitator
Primary DI
05707480153671
Version / Model
520611000E
Catalog Number
520611000E
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-12
Public Version
1
Public Version Date
2024-02-20
Public Version Status
New
Public Device Record Key
111f5b13-2fe8-442f-93b2-e4b4fcc793a2

Device Description

Single Patient Use Resuscitator

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
MR Conditional
Direct Marking Exempt
No
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
No

Product Codes

Code Name
OEV Cardiopulmonary resuscitation aid kit

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 05707480153688
Primary 05707480153671

Customer Contacts

Phone
+14107686464

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-18 – 50 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius