← Back to catalogue

Ssd-102

FDA UDI

Class II (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
SSD-102 FDA UDI
Generic Name
Endoscope washer-disinfector (chemical) FDA UDI
Device Name
SSD Endoscope Reprocessor FDA UDI
Model / Reference
SSD-102 FDA UDI
Description
SSD Endoscope Reprocessor FDA UDI

Identifiers

Catalog Number
SSD2007 FDA UDI
Primary DI / UDI-DI
00677964035647 FDA UDI
510(k) Number
K914145 FDA UDI
FDA Product Code
FEB FDA UDI
GMDN Term
Endoscope washer-disinfector (chemical) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Ssd-102 by Medivators Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

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
Medivators Inc.

Sources (1)

  • FDA UDI cb963a33-487a-4fa2-a070-affa8fa85555 37 fields · synced Jun 8, 2026