Strauss Surgical

FDA UDI

Class II (US FDA UDI)

by American Medical Endoscopy

Identity

Trade Name: Strauss Surgical FDA UDI
Generic Name: Endoscope channel support kit FDA UDI
Model / Reference: STS-ACC-6000-SCOCK FDA UDI

Identifiers

Primary DI / UDI-DI: 00851925007267 FDA UDI
510(k) Number: K992527 FDA UDI
FDA Product Code: FGB FDA UDI
GMDN Term: Endoscope channel support kit 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Endoscope channel support kit

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

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Cleared under the same submission

K992527 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: American Medical Endoscopy

Sources (1)

FDA UDI 826b9db3-936f-453d-9367-de0f46fe3206 33 fields · synced May 30, 2026