FDA UDI Not in Commercial Distribution 🇺🇸 United States

SPUR® II Adult Resuscitatorw / Pressure Limiting Valve and expiratory

DI: 05707480134069 · Model: 524611017 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SPUR® II Adult Resuscitatorw / Pressure Limiting Valve and expiratory
Primary DI
05707480134069
Version / Model
524611017
Catalog Number
524611017
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-05
Public Version
3
Public Version Date
2018-06-28
Public Version Status
Update
Public Device Record Key
b9421a21-037c-4eb1-9124-f762323213bb
Distribution End Date
2018-06-27

Device Description

Ambu SPUR II Adult Bag Res.

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
Package 05707480134052
Primary 05707480134069

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