FDA UDI Not in Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867084148 · Model: ABS-2001-01 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867084148
Version / Model
ABS-2001-01
Catalog Number
ABS-2001-01
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-15
Public Version
9
Public Version Date
2024-01-31
Public Version Status
Update
Public Device Record Key
e3562a77-c05b-428d-8243-0e42a106b4ea
Distribution End Date
2017-02-15

Device Description

STIMUBLAST PUTTY, 1CC

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
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBP Filler, bone void, osteoinduction (w/o human growth factor)

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00888867084148
Secondary M150ABS2001010

Customer Contacts