← Back to catalogue

Paragon

FDA UDI

Class II (US FDA UDI)

by Global Manufacturing Technology Pty Limited

Identity

Trade Name
Paragon FDA UDI
Generic Name
Press-fit hip femur prosthesis, one-piece FDA UDI
Device Name
Paragon Stem Standard Sz 5 HA FDA UDI
Model / Reference
GM08001-206-05 FDA UDI
Description
Paragon Stem Standard Sz 5 HA FDA UDI

Identifiers

Catalog Number
GM08001-206-05 FDA UDI
Primary DI / UDI-DI
09340499002064 FDA UDI
510(k) Number
K123782 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
GMDN Term
Press-fit hip femur prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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: Press-fit hip femur prosthesis, one-piece

Paragon by Global Manufacturing Technology Pty Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit hip femur prosthesis, one-piece.

Cleared under the same submission

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 77d5cb05-0beb-4185-9a88-f8a275533ee7 37 fields · synced May 30, 2026