Identity
- Trade Name
- Integra® Jarit® FDA UDI
- Generic Name
- Eye spud FDA UDI
- Device Name
- Integra® Jarit® Foreign Body Needle, 4-3/4", 2mm Blade, Curved FDA UDI
- Model / Reference
- 350325 FDA UDI
- Description
- Integra® Jarit® Foreign Body Needle, 4-3/4", 2mm Blade, Curved FDA UDI
Identifiers
- Catalog Number
- 350-325 FDA UDI
- Primary DI / UDI-DI
- 10381780166054 FDA UDI
- FDA Product Code
- HNA FDA UDI
- GMDN Term
- Eye spud 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: Eye spud
Integra® Jarit® by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye spud.
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- MR PHACO — Crestpoint Management Ltd. · Class I
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- Ambler Surgical — Ambler Surgical, LLC · Class I
- Spud — Katena Products, Inc. · Class I
- Spud — Katena Products, Inc. · 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 |
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Manufacturer
- Manufacturer
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 331ff704-05a6-49f2-a3fe-6640e18fbe78 36 fields · synced Jun 9, 2026