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Dynasty

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Dynasty FDA UDI
Generic Name
Metallic acetabulum prosthesis FDA UDI
Device Name
DYNASTY® BF SHELL PRIMARY 56MM GROUP F FDA UDI
Model / Reference
DBFPGF56 FDA UDI
Description
DYNASTY® BF SHELL PRIMARY 56MM GROUP F FDA UDI

Identifiers

Catalog Number
DBFPGF56 FDA UDI
Primary DI / UDI-DI
M684DBFPGF561 FDA UDI
FDA Product Code
JDI FDA UDI
LZO FDA UDI
MBL FDA UDI
GMDN Term
Metallic acetabulum prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3353 FDA UDI
888.3358 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 56 Millimeter FDA UDI

Category: Metallic acetabulum prosthesis

Dynasty by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic acetabulum prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd9a9dd4-f579-4356-85ee-f61436327b0d 36 fields · synced Jun 9, 2026