FDA UDI In Commercial Distribution 🇺🇸 United States

GENTEC®

DI: 06970966661925 · Model: 882VR-300-OE-D · GENTEC(SHANGHAI)CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GENTEC®
Primary DI
06970966661925
Version / Model
882VR-300-OE-D
Company Name
GENTEC(SHANGHAI)CORPORATION
Labeler DUNS
545287658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-01
Public Version
3
Public Version Date
2020-05-13
Public Version Status
Update
Public Device Record Key
a7e4f7a2-de24-456e-8d1b-8aea1de44737

Device Description

882VR series suction regulator is a suction regulator .It can be used for medical suction and enables the clinician to control the level of negative pressure for the operation of pharyngeal aspiration, tracheal suctioning etc.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
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
37783 Tracheal suction vacuum regulator

Identifiers

Type ID
Primary 06970966661925