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Strauss Surgical

FDA UDI

Class II (US FDA UDI)

by American Medical Endoscopy

Identity

Trade Name
Strauss Surgical FDA UDI
Generic Name
Resectoscope FDA UDI
Model / Reference
STS-URO-100-122-QL FDA UDI

Identifiers

Primary DI / UDI-DI
00810143890860 FDA UDI
510(k) Number
K173070 FDA UDI
FDA Product Code
FAJ FDA UDI
GMDN Term
Resectoscope 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

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

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: Resectoscope

Strauss Surgical by American Medical Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resectoscope.

Cleared under the same submission

K173070 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
American Medical Endoscopy

Sources (1)

  • FDA UDI 30746391-fda6-4a3d-b27b-4b165e9f9c08 33 fields · synced May 30, 2026