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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
Lacrimal intubation set FDA UDI
Device Name
V. Mueller CRAWFORD LACRIMAL INTUBATION SET, TWO OLIVE TIP PROBES .6MM DIA X 150MM LG ATTACHED TO 300MM LG SILIC TBE FDA UDI
Model / Reference
OP0918-851 FDA UDI
Description
V. Mueller CRAWFORD LACRIMAL INTUBATION SET, TWO OLIVE TIP PROBES .6MM DIA X 150MM LG ATTACHED TO 300MM LG SILIC TBE FDA UDI

Identifiers

Catalog Number
OP0918851 FDA UDI
Primary DI / UDI-DI
10885403094866 FDA UDI
FDA Product Code
HNL FDA UDI
GMDN Term
Lacrimal intubation set 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: Lacrimal intubation set

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

Similar devices

Also classified as Lacrimal intubation set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI ae3d1898-de54-4672-b309-80ae149e1091 35 fields · synced Jun 6, 2026