FDA UDI In Commercial Distribution 🇺🇸 United States

Drive

DI: 00822383295985 · Model: 610-12B · Drive Devilbiss Healthcare
Product Codes
2
GMDN Terms
3
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Drive
Primary DI
00822383295985
Version / Model
610-12B
Company Name
Drive Devilbiss Healthcare
Labeler DUNS
867673159
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
10
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
45c723cd-e2d7-4014-ad3c-47dac21c0371

Device Description

Suction Canister

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ BOTTLE, COLLECTION, VACUUM
GAZ TUBING, NONINVASIVE

GMDN Terms

Code Name
44943 Surgical suction system collection container, reusable
34858 Surgical suction system collection container, single-use
16779 Suction/irrigation tubing, single-use

Identifiers

Type ID
Package 10822383295982
Primary 00822383295985