FDA UDI Not in Commercial Distribution 🇺🇸 United States

n/a

DI: 00874750007110 · Model: 3830 · HANS RUDOLPH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n/a
Primary DI
00874750007110
Version / Model
3830
Catalog Number
112946
Company Name
HANS RUDOLPH, INC.
Labeler DUNS
007131725
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
6
Public Version Date
2023-06-30
Public Version Status
Update
Public Device Record Key
4284787f-5926-4b50-a048-4c9087b270d4
Distribution End Date
2023-06-30

Device Description

3830B PNT/HTRSHELL/CONN ASSY

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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JAX Pneumotachometer

GMDN Terms

Code Name
35245 Pneumotachograph

Identifiers

Type ID
Primary 00874750007110