FDA UDI In Commercial Distribution 🇺🇸 United States

Ventlab

DI: 10889483101346 · Model: HS4351-M · VENTLAB, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Ventlab
Primary DI
10889483101346
Version / Model
HS4351-M
Company Name
VENTLAB, LLC
Labeler DUNS
038305402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2eb34c63-ff41-44d0-94ad-c61834dad634

Device Description

1/2 L HYPERINFLATION SYS W/ MANO & SIZE 3 BLOW MOLD MASK

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
NHK Resuscitator,Manual,Non Self-Inflating

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 20889483101343
Primary 10889483101346

Customer Contacts

Phone
800-433-2797

Device Sizes

Type Value Unit Text
Total Volume .5 Liter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature. Do not get wet.