Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Periocular/lacrimal retractor, self-retaining FDA UDI
- Device Name
- V. Mueller AGRIKOLA LACRIMAL SAC RETRACTOR 3 X 3 SEMI-SHARP PRONGS OVERALL LENGTH 1-5/8 inches 4.1CM FDA UDI
- Model / Reference
- OP330 FDA UDI
- Description
- V. Mueller AGRIKOLA LACRIMAL SAC RETRACTOR 3 X 3 SEMI-SHARP PRONGS OVERALL LENGTH 1-5/8 inches 4.1CM FDA UDI
Identifiers
- Catalog Number
- OP330 FDA UDI
- Primary DI / UDI-DI
- 10885403096686 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Periocular/lacrimal retractor, self-retaining 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
Moist Heat or Steam Sterilization FDA UDI
Category: Periocular/lacrimal retractor, self-retaining
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, self-retaining.
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI a1fa371f-878f-4dd8-8e78-fcb57cf80458 35 fields · synced Jun 8, 2026