FDA UDI Not in Commercial Distribution 🇺🇸 United States

6000 NDGB

DI: 00817136025834 · Model: 6000 · HANS RUDOLPH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
6000 NDGB
Primary DI
00817136025834
Version / Model
6000
Catalog Number
CR1999
Company Name
HANS RUDOLPH, INC.
Labeler DUNS
007131725
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-05
Public Version
3
Public Version Date
2023-06-30
Public Version Status
Update
Public Device Record Key
2e3a659a-5fd0-439a-8296-9c945d6fff8e
Distribution End Date
2023-06-30

Device Description

NDGB 20L DUAL BAG 2 ON/OFF VLV

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
No
PM Exempt
Yes
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
BTC Bag, Reservoir

GMDN Terms

Code Name
33513 Exhaled-gas sample collector, non-electronic

Identifiers

Type ID
Primary 00817136025834