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Mini and Micro Fragments Reconstruction System - GMReis

FDA UDI

Class II (US FDA UDI)

by Gm Dos Reis Industria E Comercio Ltda

Identity

Trade Name
Mini and Micro Fragments Reconstruction System - GMReis FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference
LEFT VERSALOCK FLP PLATE WITH VOLAR RIM FRAGMENT FIXATION FDA UDI

Identifiers

Catalog Number
180-135-E FDA UDI
Primary DI / UDI-DI
07899258695754 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 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

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Mini and Micro Fragments Reconstruction System - GMReis by Gm Dos Reis Industria E Comercio Ltda — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c47a941f-f3fb-49b7-acf7-83338c7b3ca7 33 fields · synced Jun 1, 2026