← Back to catalogue

Reference Plate Cover

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
REFERENCE PLATE COVER FDA UDI
Generic Name
Sensor holder, single-use FDA UDI
Device Name
REFERENCE PLATE COVER FDA UDI
Model / Reference
MAJ-1880 FDA UDI
Description
REFERENCE PLATE COVER FDA UDI

Identifiers

Catalog Number
N3806500 FDA UDI
Primary DI / UDI-DI
04953170305719 FDA UDI
FDA Product Code
FDF FDA UDI
FDA FDA UDI
PGU FDA UDI
GMDN Term
Sensor holder, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sensor holder, single-use

Reference Plate Cover by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sensor holder, single-use.

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 729b1754-764c-4878-a451-adb9d1ae6e5e 35 fields · synced May 30, 2026