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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
Rigid endoscopic stone-retrieval forceps, reusable FDA UDI
Model / Reference
STS-URO-082-90 FDA UDI

Identifiers

Primary DI / UDI-DI
00850033250671 FDA UDI
FDA Product Code
LQC FDA UDI
GMDN Term
Rigid endoscopic stone-retrieval forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4500 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

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 endoscopic stone-retrieval forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic stone-retrieval forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b897643f-ad4f-47b6-847d-95731aec9f58 32 fields · synced May 30, 2026