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BoneSync Fast-Setting Drillable Calcium Phosphate Cement

FDA UDI

Class II (US FDA UDI)

by Dsm Biomedical, Inc.

Identity

Trade Name
BoneSync Fast-Setting Drillable Calcium Phosphate Cement FDA UDI
Generic Name
Bone matrix implant, composite FDA UDI
Device Name
Fast-Setting Drillable Calcium Phosphate Cement FDA UDI
Model / Reference
21003-03 FDA UDI
Description
Fast-Setting Drillable Calcium Phosphate Cement FDA UDI

Identifiers

Catalog Number
ABS-3103 FDA UDI
Primary DI / UDI-DI
00812337029209 FDA UDI
FDA Product Code
MQV FDA UDI
OIS FDA UDI
GMDN Term
Bone matrix implant, composite FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Bone matrix implant, composite

BoneSync Fast-Setting Drillable Calcium Phosphate Cement by Dsm Biomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, composite.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c6931b6c-f419-47df-a4fc-879cb20a6934 35 fields · synced May 30, 2026