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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
Ophthalmic suture scissors FDA UDI
Device Name
V. Mueller UTILITY SCISSORS RIBBON STYLE HANDLES CVD BLDS, 2.5CM FROM MID-SCREW OVERALL LENGTH 4 inches 10.2CM FDA UDI
Model / Reference
OP5726 FDA UDI
Description
V. Mueller UTILITY SCISSORS RIBBON STYLE HANDLES CVD BLDS, 2.5CM FROM MID-SCREW OVERALL LENGTH 4 inches 10.2CM FDA UDI

Identifiers

Catalog Number
OP5726 FDA UDI
Primary DI / UDI-DI
10885403099748 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Ophthalmic suture scissors 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: Ophthalmic suture scissors

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

Similar devices

Also classified as Ophthalmic suture scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI b7527d70-f5a3-45a7-b2b6-c9adf9bcb929 35 fields · synced Jun 8, 2026