← Back to catalogue

RTK10161 Room Turnover Kit

FDA UDI

Class I (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name
RTK10161 Room Turnover Kit FDA UDI
Generic Name
Operating room turnover kit FDA UDI
Device Name
RTK10161 Room Turnover Kit FDA UDI
Model / Reference
RTK10161 FDA UDI
Description
RTK10161 Room Turnover Kit FDA UDI

Identifiers

Catalog Number
RTK10161 FDA UDI
Primary DI / UDI-DI
00787551011883 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Operating room turnover kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating room turnover kit

RTK10161 Room Turnover Kit by Xodus Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room turnover kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Xodus Medical, Inc.

Sources (1)

  • FDA UDI 6d995f70-ff40-4118-8c94-1f559095125a 35 fields · synced Jun 6, 2026