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Strauss Surgical

FDA UDI

Class I (US FDA UDI)

by American Medical Endoscopy

Identity

Trade Name
Strauss Surgical FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, reusable FDA UDI
Model / Reference
STS-URO-GRA-70-40AL FDA UDI

Identifiers

Primary DI / UDI-DI
00850024135765 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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
MRI Safety
MR Safe FDA UDI

Category: Flexible endoscopic biopsy forceps, reusable

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

Similar devices

Also classified as Flexible endoscopic biopsy forceps, reusable.

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 69bdeadc-5a38-47b7-9b82-bbffcd4fa14b 32 fields · synced May 30, 2026