FDA UDI In Commercial Distribution 🇺🇸 United States

InterGro DBM Plus

DI: 00888480585206 · Model: DBM050 · Biomet Orthopedics, LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
InterGro DBM Plus
Primary DI
00888480585206
Version / Model
DBM050
Catalog Number
DBM050
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4bc0f919-387c-4f88-8f3f-b964c1041928

Device Description

Porous Hydroxyapatite Bone Graft Substitute

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
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
GXP Methyl Methacrylate For Cranioplasty
MQV Filler, Bone Void, Calcium Compound
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Primary 00888480585206

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify STERILE Granules, 15 cc