FDA UDI In Commercial Distribution 🇺🇸 United States

SPUR® II Pediatric ResuscitatorSingle Patient Use Resuscitator

DI: 05707480105328 · Model: 530215031 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SPUR® II Pediatric ResuscitatorSingle Patient Use Resuscitator
Primary DI
05707480105328
Version / Model
530215031
Catalog Number
530215031
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
3
Public Version Date
2021-06-01
Public Version Status
Update
Public Device Record Key
3d341f1c-7326-4f80-8a4c-ecfa7e4a3777
Distribution End Date
2026-05-31

Device Description

Inf &Todd Face Mask, Disp Manometer, Disp PEEP Valve 12/cs

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 05707480105328
Package 05707480105335

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Device Size Text, specify Pediatric

Storage Conditions

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