FDA UDI In Commercial Distribution 🇺🇸 United States

Breathing Bag

DI: 10641043553923 · Model: 10-55392 · MERCURY ENTERPRISES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Breathing Bag
Primary DI
10641043553923
Version / Model
10-55392
Company Name
MERCURY ENTERPRISES, INC.
Labeler DUNS
032705659
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-30
Public Version
1
Public Version Date
2018-10-01
Public Version Status
New
Public Device Record Key
17c1cb25-5792-4f69-8877-291a65abfd2a

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
No
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 30641043553927
Primary 10641043553923

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K001714 000