Identity
- Trade Name
- MSI Precision Specialty Instruments FDA UDI
- Generic Name
- Ophthalmic knife, reusable FDA UDI
- Device Name
- Cataract Diamond Knife (Black CVD Diamond Blade) On A Black Gold Titanium Handle, 1mm 75 Degrees Lance Angled Dop J-Slot Bayonet Handle Design, Blade Dimensions 1mm Wide By 0.17mm Thick By 6mm Long FDA UDI
- Model / Reference
- PABD1010A FDA UDI
- Description
- Cataract Diamond Knife (Black CVD Diamond Blade) On A Black Gold Titanium Handle, 1mm 75 Degrees Lance Angled Dop J-Slot Bayonet Handle Design, Blade Dimensions 1mm Wide By 0.17mm Thick By 6mm Long FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00194613101336 FDA UDI
- FDA Product Code
- HNN FDA UDI
- GMDN Term
- Ophthalmic knife, 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic knife, reusable
MSI Precision Specialty Instruments by Med Saver, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic knife, reusable.
- MICRO FEATHER OPHTHALMIC SCALPEL with aluminum handle — FEATHER SAFETY RAZOR CO., LTD. · Class I
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- Mastel Precision Surgical Instruments, Inc. — MASTEL SURGICAL INC. · Class I
- Mastel Precision Surgical Instruments, Inc. — MASTEL SURGICAL INC. · Class I
- Ophthalmic Knife — Katena Products, Inc. · Class I
- Walcott Rx Products — Walcott Rx Product Inc · Class I
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- Wexler Surgical, Inc. — Wexler 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
- Med Saver, Inc.
Sources (1)
- FDA UDI 8c9ac10a-2d1e-4499-a8bd-1cad7de97d1b 34 fields · synced Jun 8, 2026