FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00874750001293 · Model: 7600 · HANS RUDOLPH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00874750001293
Version / Model
7600
Catalog Number
113380
Company Name
HANS RUDOLPH, INC.
Labeler DUNS
007131725
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-16
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
28f65935-43bc-4c20-ab4a-1d6c85efecce

Device Description

7600 LG FF W/AAV 22ID QREL HDG

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Yes
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
BZD Ventilator, Non-Continuous (Respirator)

GMDN Terms

Code Name
57814 CPAP/BPAP face mask, reusable

Identifiers

Type ID
Primary 00874750001293

Premarket Submissions

Submission Number Supplement Number
K030822 000