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Elmed Incorporated

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED INCORPORATED FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
OUTER SHEATH FOR CONTINUOUS FLOW WITH SUCTION CONTROL STOPCOCK, 7MM DIA. FDA UDI
Model / Reference
51400-16B FDA UDI
Description
OUTER SHEATH FOR CONTINUOUS FLOW WITH SUCTION CONTROL STOPCOCK, 7MM DIA. FDA UDI

Identifiers

Catalog Number
51400-16B FDA UDI
Primary DI / UDI-DI
00198506084454 FDA UDI
FDA Product Code
KOA FDA UDI
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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: Endoscope sheath, reusable

Elmed Incorporated by Elmed Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope sheath, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 949fe5d1-51c7-4c21-b706-7de354bac446 35 fields · synced May 30, 2026