V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: Hand-held surgical retractor, reusable FDA UDI
Device Name: V. Mueller MEYERDING RETRACTOR SHARP TOOTHED EDGE BLADE 5/8X2 inches 1.6X5.1CM WIDE OVERALL LENGTH 8-1/2 inches 21.6CM FDA UDI
Model / Reference: NL5132 FDA UDI
Description: V. Mueller MEYERDING RETRACTOR SHARP TOOTHED EDGE BLADE 5/8X2 inches 1.6X5.1CM WIDE OVERALL LENGTH 8-1/2 inches 21.6CM FDA UDI

Identifiers

Catalog Number: NL5132 FDA UDI
Primary DI / UDI-DI: 10885403081132 FDA UDI
FDA Product Code: HAO FDA UDI
GMDN Term: Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4535 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held surgical retractor, reusable

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

Similar devices

Also classified as Hand-held surgical retractor, reusable.

ATLAS — ATLAS CERRAHİ ALETLER LTD. ŞTİ. · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
MİKRO — SAMSUN MİKRO CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ · Class I
Gimmi — Gimmi GmbH · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
Sklar® — Sklar Corporation · Class I
BIOCOMPOSITE PLUS ANCHOR Ø3, 5 MM W/NEEDLE — BMT BAPS BİYO MALZEME SANAYİ VE TİCARET ANONİM ŞİRKETİ · Class III
Spreizer / Spreader — REDA Instrumente GmbH · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI 54b27df7-586d-449a-b657-f965a2ccceed 35 fields · synced Jun 8, 2026