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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Rib spreader, reusable FDA UDI
Device Name
V. Mueller WILSON RIB SPREADER INFANT BLADES 26X30MM WIDE ARM LENGTH 4 inches 10.2CM SPREAD 3-7/8 inches 9.8CM FDA UDI
Model / Reference
CH1250 FDA UDI
Description
V. Mueller WILSON RIB SPREADER INFANT BLADES 26X30MM WIDE ARM LENGTH 4 inches 10.2CM SPREAD 3-7/8 inches 9.8CM FDA UDI

Identifiers

Catalog Number
CH1250 FDA UDI
Primary DI / UDI-DI
10885403023460 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Rib spreader, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rib spreader, reusable

V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rib spreader, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 6ff02574-a85f-467a-8995-12dd1ac54c4a 35 fields · synced Jun 8, 2026