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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
Conjunctival scissors, reusable FDA UDI
Device Name
V. Mueller TORCHIA CONJUNCTIVAL SCISSORS SERRATED BLADE BLADES 11 MM FROM MID-SCREW OVERALL LENGTH 4 inches 10.2 CM FDA UDI
Model / Reference
OP5667 FDA UDI
Description
V. Mueller TORCHIA CONJUNCTIVAL SCISSORS SERRATED BLADE BLADES 11 MM FROM MID-SCREW OVERALL LENGTH 4 inches 10.2 CM FDA UDI

Identifiers

Catalog Number
OP5667 FDA UDI
Primary DI / UDI-DI
10885403099632 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Conjunctival scissors, 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: Conjunctival scissors, reusable

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

Similar devices

Also classified as Conjunctival scissors, 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 254ef666-a517-4d07-b4dc-a5c1af7c39a0 35 fields · synced Jun 6, 2026