FDA UDI In Commercial Distribution 🇺🇸 United States

STIMUBLAST®

DI: M536ABS2004031 · Model: ABS-2004-03 · ALLOSOURCE
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STIMUBLAST®
Primary DI
M536ABS2004031
Version / Model
ABS-2004-03
Catalog Number
ABS-2004-03
Company Name
ALLOSOURCE
Labeler DUNS
946808136
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8176e1a0-a00f-4fd6-a693-83e96d23902b

Device Description

STIMUBLAST® CB DBM Paste, 3cc

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Primary M536ABS2004031

Device Sizes

Type Value Unit Text
Device Size Text, specify 3 cc

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius