FDA UDI In Commercial Distribution 🇺🇸 United States

Ambu

DI: 10889483222164 · Model: 900-000-602 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Ambu
Primary DI
10889483222164
Version / Model
900-000-602
Catalog Number
900-000-602
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-19
Public Version
2
Public Version Date
2026-04-20
Public Version Status
Update
Public Device Record Key
b76592b5-f8f8-4e43-8cd3-a42d6ce04700

Device Description

Ambu Disposable Hyperinflation System, Hyperinflation System, 2 L Bag, 7' O2 and Pressure Lines

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZR Mixer, Breathing Gases, Anesthesia Inhalation

GMDN Terms

Code Name
37706 Ventilator breathing circuit, single-use

Identifiers

Type ID
Package 20889483222161
Primary 10889483222164
Previous 05707480103201

Customer Contacts