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Baby Gorilla/Gorilla Plating System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Baby Gorilla/Gorilla Plating System FDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
MTP Spin Guard Male Reamer Protector Sleeve, 21mm FDA UDI
Model / Reference
P01-911-2101 FDA UDI
Description
MTP Spin Guard Male Reamer Protector Sleeve, 21mm FDA UDI

Identifiers

Catalog Number
P01-911-2101 FDA UDI
Primary DI / UDI-DI
00889795035028 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic implantation sleeve, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic implantation sleeve, reusable

Baby Gorilla/Gorilla Plating System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantation sleeve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI db5224b7-97b2-4919-981a-e02b8bede1af 34 fields · synced May 31, 2026