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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
Periocular/lacrimal retractor, hand-held, reusable FDA UDI
Device Name
V. Mueller ORBITAL RETRACTOR BLADE 16MM DEEP X 25MM LONG OVERALL LENGTH 7-1/4 inches 18.4CM FDA UDI
Model / Reference
OP0906-321 FDA UDI
Description
V. Mueller ORBITAL RETRACTOR BLADE 16MM DEEP X 25MM LONG OVERALL LENGTH 7-1/4 inches 18.4CM FDA UDI

Identifiers

Catalog Number
OP0906321 FDA UDI
Primary DI / UDI-DI
10885403203152 FDA UDI
FDA Product Code
HNI FDA UDI
GMDN Term
Periocular/lacrimal retractor, hand-held, 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: Periocular/lacrimal retractor, hand-held, reusable

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

Similar devices

Also classified as Periocular/lacrimal retractor, hand-held, 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 ca0e5d5f-a02f-4d2a-a52c-bdc031abbb7b 35 fields · synced Jun 8, 2026