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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
Self-retaining surgical retractor, reusable FDA UDI
Device Name
BRAWLEY SCLERAL WOUND RETRACTOR, NICKEL SILVER LIGHT, DELICATE, NON-MAGNETIC OVERALL LENGTH 1-1/4 inches3.2CM FDA UDI
Model / Reference
OP370 FDA UDI
Description
BRAWLEY SCLERAL WOUND RETRACTOR, NICKEL SILVER LIGHT, DELICATE, NON-MAGNETIC OVERALL LENGTH 1-1/4 inches3.2CM FDA UDI

Identifiers

Catalog Number
OP370 FDA UDI
Primary DI / UDI-DI
10885403096716 FDA UDI
FDA Product Code
HNI FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Self-retaining 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 Self-retaining surgical retractor, 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 ec31f510-2daf-4469-abde-22415bae031d 35 fields · synced Jun 8, 2026