← Back to catalogue

Dbx®

FDA UDI

Class II (US FDA UDI)

by Musculoskeletal Transplant Foundation

Identity

Trade Name
DBX® FDA UDI
Generic Name
Bone matrix implant, human-derived FDA UDI
Device Name
DBM Putty, 2.5cc FDA UDI
Model / Reference
030025 FDA UDI
Description
DBM Putty, 2.5cc FDA UDI

Identifiers

Catalog Number
030025 FDA UDI
Primary DI / UDI-DI
W4184030025T0473 FDA UDI
FDA Product Code
NUN FDA UDI
GMDN Term
Bone matrix implant, human-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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

Category: Bone matrix implant, human-derived

Dbx® by Musculoskeletal Transplant Foundation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, human-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9cb53521-d1ee-469e-9ce3-a0636e578559 36 fields · synced May 30, 2026