FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10193489136173 · Model: RTDC3HDH · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10193489136173
Version / Model
RTDC3HDH
Catalog Number
RTDC3HDH
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-04
Public Version
1
Public Version Date
2022-03-14
Public Version Status
New
Public Device Record Key
23e06a68-1f48-4958-95e0-ad79b3c81c91

Device Description

REGULATOR,SUCTION,DIG,CONT,H TRP,DISS HT

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
Yes
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
KDP REGULATOR, VACUUM

GMDN Terms

Code Name
44809 Vacuum suction regulator/regulation set, general-purpose

Identifiers

Type ID
Primary 10193489136173

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
55 – 85 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity