FDA UDI In Commercial Distribution 🇺🇸 United States

Post Medical, Inc.

DI: B309PMSM9500 · Model: PMSM-950 · POST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Post Medical, Inc.
Primary DI
B309PMSM9500
Version / Model
PMSM-950
Company Name
POST MEDICAL, INC.
Labeler DUNS
968012943
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
4
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
96d64be4-e843-4636-9f03-2a4a287da9d9

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
No
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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
35429 Sharps container

Identifiers

Type ID
Package B309PMSM9501
Primary B309PMSM9500

Premarket Submissions

Submission Number Supplement Number
K990371 000