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Rhausler

FDA UDI

Class II (US FDA UDI)

by Rhausler, Inc.

Identity

Trade Name
Rhausler FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
PLAGE IMPLANT AND INSTRUMENT TRAY FDA UDI
Model / Reference
C-7091 FDA UDI
Description
PLAGE IMPLANT AND INSTRUMENT TRAY FDA UDI

Identifiers

Catalog Number
C-7091 FDA UDI
Primary DI / UDI-DI
08500591410629 FDA UDI
510(k) Number
K111272 FDA UDI
FDA Product Code
OVE FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Metallic spinal interbody fusion cage

Rhausler by Rhausler, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rhausler, Inc.

Sources (1)

  • FDA UDI baac1732-0bab-4138-a79b-0a5f4d8681e6 35 fields · synced May 30, 2026