FDA UDI In Commercial Distribution 🇺🇸 United States

Precision Medical Inc.

DI: 00855887006092 · Model: PM3300 SERIES · Precision Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Precision Medical Inc.
Primary DI
00855887006092
Version / Model
PM3300 SERIES
Company Name
Precision Medical, Inc.
Labeler DUNS
112569116
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-18
Public Version
5
Public Version Date
2021-04-22
Public Version Status
Update
Public Device Record Key
7e4db01a-b42f-48c4-821b-b4818aadbd3d

Device Description

PM3300 SERIES,VAC REG,INTERMITTENT,200MMHG

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
No
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 00855887006092

Premarket Submissions

Submission Number Supplement Number
K944479 000