← Back to catalogue

Instrument Tray No Clamp

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
INSTRUMENT TRAY NO CLAMP FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
INSTRUMENT TRAY NO CLAMP FDA UDI
Model / Reference
6-060-01-1 FDA UDI
Description
INSTRUMENT TRAY NO CLAMP FDA UDI

Identifiers

Primary DI / UDI-DI
10841736113674 FDA UDI
FDA Product Code
LWG FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument tray, reusable

Instrument Tray No Clamp by Skytron, LLC — 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
Skytron, LLC

Sources (1)

  • FDA UDI 74d30d57-fd83-414d-a7a3-220a94711b09 34 fields · synced May 30, 2026