FDA UDI In Commercial Distribution 🇺🇸 United States

Precision Medical

DI: 00850027043753 · Model: PMX900-50 · Precision Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Precision Medical
Primary DI
00850027043753
Version / Model
PMX900-50
Company Name
Precision Medical, Inc.
Labeler DUNS
112569116
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-16
Public Version
1
Public Version Date
2024-12-24
Public Version Status
New
Public Device Record Key
a8cc6b1a-4bc1-4ce6-988f-2fb06de9f86c

Device Description

VAC TRAP,FILTERED,BOX OF 50

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
63649 General-purpose surgical suction system, vacuum

Identifiers

Type ID
Primary 00850027043753

Customer Contacts

Phone
6102626090