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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
Neurosurgical bone flap elevator FDA UDI
Device Name
V. Mueller Neuro/Spine SHADOW-LINE MCCULLOCH DOUBLE-ENDED BLUNT ELEVATOR BLADE 5.6MM WIDE WORKING LENGTH 9 inches 22.9CM FDA UDI
Model / Reference
S-1992 FDA UDI
Description
V. Mueller Neuro/Spine SHADOW-LINE MCCULLOCH DOUBLE-ENDED BLUNT ELEVATOR BLADE 5.6MM WIDE WORKING LENGTH 9 inches 22.9CM FDA UDI

Identifiers

Catalog Number
S1992 FDA UDI
Primary DI / UDI-DI
10885403118968 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
Neurosurgical bone flap elevator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Neurosurgical bone flap elevator

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

Similar devices

Also classified as Neurosurgical bone flap elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 779c412b-0fad-4f01-8650-b929dc33959d 35 fields · synced Jun 8, 2026