FDA UDI In Commercial Distribution 🇺🇸 United States

SPUR® Adult Resuscitator

DI: 05707480154036 · Model: 520211061E · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
SPUR® Adult Resuscitator
Primary DI
05707480154036
Version / Model
520211061E
Catalog Number
520211061E
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-20
Public Version
2
Public Version Date
2026-01-30
Public Version Status
Update
Public Device Record Key
dcf0ecb0-04cc-43f7-9f8d-d87b63a6c64f

Device Description

SPUR II Adult Bag Res, Med Mask, PEEP, Exp Filter, GSL

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
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 05707480154029
Primary 05707480154036

Customer Contacts

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