← Back to catalogue

Osteotec CBG Tray, empty

FDA UDI

Class I (US FDA UDI)

by Osteotec, Ltd.

Identity

Trade Name
Osteotec CBG Tray, empty FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Osteotec CBG Instrument Tray, empty FDA UDI
Model / Reference
OST-CGB-TRAY FDA UDI
Description
Osteotec CBG Instrument Tray, empty FDA UDI

Identifiers

Catalog Number
OST-CGB-TRAY FDA UDI
Primary DI / UDI-DI
05060183095786 FDA UDI
FDA Product Code
OJH FDA UDI
GMDN Term
Instrument tray, 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Osteotec CBG Tray, empty by Osteotec, Ltd. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Osteotec, Ltd.

Sources (1)

  • FDA UDI 2ea78165-67e6-4933-ae2b-2ce5addb0442 34 fields · synced Jun 8, 2026