FDA UDI In Commercial Distribution 🇺🇸 United States

SPUR® II Adult ResuscitatorSingle Patient Use Resuscitator

DI: 05707480033058 · Model: 521600000 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SPUR® II Adult ResuscitatorSingle Patient Use Resuscitator
Primary DI
05707480033058
Version / Model
521600000
Catalog Number
521600000
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-19
Public Version
4
Public Version Date
2023-06-30
Public Version Status
Update
Public Device Record Key
f1f907f6-63ac-400d-ba1c-2b9490f3991c
Distribution End Date
2026-05-31

Device Description

Ambu SPUR II Adult with open reservoir 40 and without face mask. 6 pcs/box

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
BTM Ventilator, emergency, manual (resuscitator)

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Primary 05707480033058
Package 05707480017324

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 60 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
-18 – 50 Degrees Celsius