Strauss Surgical

FDA UDI

Class I (US FDA UDI)

by American Medical Endoscopy

Identity

Trade Name: Strauss Surgical FDA UDI
Generic Name: Bone curette, reusable FDA UDI
Model / Reference: STS-ART-40-0018 FDA UDI

Identifiers

Primary DI / UDI-DI: 00850024135710 FDA UDI
FDA Product Code: NBH FDA UDI
GMDN Term: Bone curette, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1100 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Bone curette, reusable

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

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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 I	Pending data

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Manufacturer

Manufacturer: American Medical Endoscopy

Sources (1)

FDA UDI 2c895c44-751d-4a3a-b63c-e588b77d5341 32 fields · synced Jun 8, 2026