FDA UDI Not in Commercial Distribution 🇺🇸 United States

PROSPACE®

DI: 04046963142148 · Model: SJ286P · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROSPACE®
Primary DI
04046963142148
Version / Model
SJ286P
Catalog Number
SJ286P
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
2ae91aff-73cf-45ad-a271-ed107883d8c4
Distribution End Date
2016-02-18

Device Description

PROSPACE PEEK IMPLANT 8° 9X10X22MM

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 04046963142148

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Degree (°) : 8.000 DEG
Device Size Text, specify Height : 9.000 MM
Device Size Text, specify Length : 22.000 MM