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Operon

FDA UDI

Class I (US FDA UDI)

by STRYKER Communications, Inc.

Identity

Trade Name
OPERON FDA UDI
Generic Name
Medical table clamp FDA UDI
Device Name
Surgical Table,INSIDE RAIL CLAMP FDA UDI
Model / Reference
OZ 7527675 FDA UDI
Description
Surgical Table,INSIDE RAIL CLAMP FDA UDI

Identifiers

Catalog Number
OZ 7527675 FDA UDI
Primary DI / UDI-DI
07613327354294 FDA UDI
FDA Product Code
GDC FDA UDI
GMDN Term
Medical table clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

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

No

FDA UDI

Category: Medical table clamp

Operon by STRYKER Communications, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical table clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 90a83a1d-4947-491b-aad8-5f320b1160a7 35 fields · synced May 30, 2026