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Gbr Modular Set

FDA UDI

Class I (US FDA UDI)

by Mc Bio Srl

Identity

Trade Name
GBR MODULAR SET FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
GBR MODULAR SET of MCBio FDA UDI
Model / Reference
9575310 FDA UDI
Description
GBR MODULAR SET of MCBio FDA UDI

Identifiers

Primary DI / UDI-DI
08057639710628 FDA UDI
FDA Product Code
EJB FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Gbr Modular Set by Mc Bio Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mc Bio Srl

Sources (1)

  • FDA UDI 1cdad7b5-28b8-4dc7-bacf-2c01b9862888 33 fields · synced Jun 6, 2026