FDA UDI In Commercial Distribution 🇺🇸 United States

Lung Diffusion Mixture

DI: 00860009502000 · Model: 1 · Roberts Oxygen Company, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Lung Diffusion Mixture
Primary DI
00860009502000
Version / Model
1
Company Name
Roberts Oxygen Company, Inc.
Labeler DUNS
791818008
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-09
Public Version
1
Public Version Date
2022-11-17
Public Version Status
New
Public Device Record Key
a4262f80-281e-42c2-a375-d3dbf54ee8b4

Device Description

Used for calibrating analyzers that measure the amount of carbon monoxide diffused through the lungs.

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BXK Gas, Calibration (Specified Concentration)

GMDN Terms

Code Name
35467 Carbon monoxide breath analyser

Identifiers

Type ID
Primary 00860009502000