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Pro Osteon 200r Granules

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
PRO OSTEON 200R GRANULES FDA UDI
Generic Name
Synthetic bone graft FDA UDI
Device Name
Resorbable Bone Graft Substitute, Granules in Syringes FDA UDI
Model / Reference
2RGS05 FDA UDI
Description
Resorbable Bone Graft Substitute, Granules in Syringes FDA UDI

Identifiers

Catalog Number
2RGS05 FDA UDI
Primary DI / UDI-DI
00888480584377 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Synthetic bone graft 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

Category: Synthetic bone graft

Pro Osteon 200r Granules by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic bone graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c588d20-14a8-4efb-861e-8f341bce8ea4 36 fields · synced May 30, 2026