FDA UDI In Commercial Distribution 🇺🇸 United States

BROSELOW™

DI: 10889483588895 · Model: 7700OIO · AIRLIFE
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BROSELOW™
Primary DI
10889483588895
Version / Model
7700OIO
Catalog Number
7700OIO
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-07
Public Version
2
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
9566ce3d-748f-469f-b27a-aa2b2b1cf51d

Device Description

BROSELOW™ INTRAOSSEOUS MODULES

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OKI Emergency Response Safety Kit

GMDN Terms

Code Name
35693 Cardiopulmonary resuscitation kit, single-use

Identifiers

Type ID
Package 30889483588899
Primary 10889483588895

Customer Contacts