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Elmed

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Rigid endoscope telescope FDA UDI
Device Name
2.9MM DIA. 25CM EOS HD MINI LAPAROSCOPE 0 DEGREE PREMIUM LENS, AUTOCLAVABLE STORZ LOCK FDA UDI
Model / Reference
52325-30S FDA UDI
Description
2.9MM DIA. 25CM EOS HD MINI LAPAROSCOPE 0 DEGREE PREMIUM LENS, AUTOCLAVABLE STORZ LOCK FDA UDI

Identifiers

Catalog Number
52325-30S FDA UDI
Primary DI / UDI-DI
00842180168626 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Rigid endoscope telescope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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: Rigid endoscope telescope

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

Similar devices

Also classified as Rigid endoscope telescope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 518ad226-b806-4467-ad14-5c5f6a9136f6 35 fields · synced May 30, 2026