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MULTICUTTER - Arthroscopic Retrograde Drill

FDA UDI

Class I (US FDA UDI)

by Gm Dos Reis Industria E Comercio Ltda

Identity

Trade Name
MULTICUTTER - Arthroscopic Retrograde Drill FDA UDI
Generic Name
Ligament reconstruction instrument set, single-use FDA UDI
Device Name
Multicutter - Arthroscopic Retrograde Drill 322 x 36 x 23mm FDA UDI
Model / Reference
MULTICUTTER - Arthroscopic Retrograde Drill FDA UDI
Description
Multicutter - Arthroscopic Retrograde Drill 322 x 36 x 23mm FDA UDI

Identifiers

Catalog Number
312-500 FDA UDI
Primary DI / UDI-DI
07899258657677 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Ligament reconstruction instrument set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ligament reconstruction instrument set, single-use

MULTICUTTER - Arthroscopic Retrograde Drill by Gm Dos Reis Industria E Comercio Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligament reconstruction instrument set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gm Dos Reis Industria E Comercio Ltda

Sources (1)

  • FDA UDI d9cb5380-78f2-43c6-937a-549baaeaf844 34 fields · synced May 30, 2026