FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoMedFlex, LLC

DI: M716AS718P0 · Model: AS-7-18P · ORTHOMEDFLEX LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
OrthoMedFlex, LLC
Primary DI
M716AS718P0
Version / Model
AS-7-18P
Catalog Number
AS-7-18P
Company Name
ORTHOMEDFLEX LLC
Labeler DUNS
034442726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-25
Public Version
3
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
ea936b2f-d47c-4cbe-8ab4-5d99ee488354

Device Description

Cement Plug, 18mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate

GMDN Terms

Code Name
38799 Polymer orthopaedic cement restrictor, non-bioabsorbable

Identifiers

Type ID
Primary M716AS718P0

Customer Contacts