Identity
- Trade Name
- Sklar Instruments FDA UDI
- Generic Name
- Ophthalmic strabismus scissors, single-use FDA UDI
- Device Name
- ECONO STERILE STRABIS SCISS CVD 4.5"STER 50 FDA UDI
- Model / Reference
- 96-2541 FDA UDI
- Description
- ECONO STERILE STRABIS SCISS CVD 4.5"STER 50 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10649111055089 FDA UDI
- FDA Product Code
- HNF FDA UDI
- GMDN Term
- Ophthalmic strabismus scissors, single-use 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Ophthalmic strabismus scissors, single-use
Sklar Instruments by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic strabismus scissors, single-use.
- Scissors Curved Strabismus 11cm — BLINK MEDICAL LIMITED · Class I
- Scissors Strabismus Straight — BLINK MEDICAL LIMITED · Class I
- Sklar Instruments — Sklar Corporation · 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
- Sklar Corporation
Sources (1)
- FDA UDI 0a80869f-4cb0-4102-9793-03087cf65aaf 33 fields · synced Jun 6, 2026