FDA UDI In Commercial Distribution 🇺🇸 United States

implacross® E PE insert 10º

DI: 04048844206949 · Model: 02343248 · implantcast GmbH
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
implacross® E PE insert 10º
Primary DI
04048844206949
Version / Model
02343248
Company Name
implantcast GmbH
Labeler DUNS
324369826
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-31
Public Version
1
Public Version Date
2018-10-01
Public Version Status
New
Public Device Record Key
3a8a943a-d424-4543-988e-9296db245290

Device Characteristics

Single Use
Yes
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
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
OQI Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented

GMDN Terms

Code Name
44362 Constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 04048844206949

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 32/48mm