FDA UDI Not in Commercial Distribution 🇺🇸 United States

A-SPACE

DI: 04038653475605 · Model: SJ129P · Aesculap AG
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
A-SPACE
Primary DI
04038653475605
Version / Model
SJ129P
Catalog Number
SJ129P
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
12
Public Version Date
2021-01-13
Public Version Status
Update
Public Device Record Key
434352ab-a182-4f2f-94ba-cae121bb35c9
Distribution End Date
2020-06-01

Device Description

A-SPACE PEEK IMPLANT SIZE L 6° 9MM

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
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 04038653475605

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Length : 28.000 MM
Device Size Text, specify Degree (°) : 6.000 DEG
Device Size Text, specify Height : 9.000 MM