FDA UDI In Commercial Distribution 🇺🇸 United States

Single Patient Use Resuscitator

DI: 05707480154418 · Model: 530213017 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Single Patient Use Resuscitator
Primary DI
05707480154418
Version / Model
530213017
Catalog Number
530213017
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
1
Public Version Date
2021-09-28
Public Version Status
New
Public Device Record Key
ef90c190-6961-423a-97e4-51bb43e6b8c8

Device Description

SPUR II Ped Bag Res, Pop-off, Tod Mask, Mano, Exp Filter

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 05707480154401
Primary 05707480154418

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Device Size Text, specify Pediatric

Storage Conditions

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