← Back to catalogue

Imperial Instrument Tray

FDA UDI

Class I (US FDA UDI)

by Imperial Surgical Ltd

Identity

Trade Name
Imperial Instrument Tray FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Instrument tray 8.25x4.33x.31" FDA UDI
Model / Reference
H-0553 FDA UDI
Description
Instrument tray 8.25x4.33x.31" FDA UDI

Identifiers

Catalog Number
H-0553 FDA UDI
Primary DI / UDI-DI
07540162041945 FDA UDI
FDA Product Code
LRP 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

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

Category: Instrument tray, reusable

Imperial Instrument Tray by Imperial Surgical 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

Sources (1)

  • FDA UDI 94682be1-2e65-4d41-a6b2-5cf2d665fa47 35 fields · synced May 30, 2026