Identity
- Trade Name
- E3571 I Curved Strabismus Scissors EUDAMEDCurved Strabismus Scissors FDA UDI
- Generic Name
- Ophthalmic strabismus scissors, reusable FDA UDI
- Device Name
- Reusable devices EUDAMED
- Model / Reference
- E3571 I EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 04058935012526 EUDAMEDFDA UDI
- Basic UDI-DI
- 4058935-000000-AC EUDAMED
- Direct Marketing DI
- 04058935012526 EUDAMED
- FDA Product Code
- HNF FDA UDI
- EMDN Code
- L01040506 TENOTOMY AND STRABISM CORRECTION SCISSORS, REUSABLE EUDAMED
- GMDN Term
- Ophthalmic strabismus scissors, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic strabismus scissors, reusable
E3571 I Curved Strabismus Scissors by Bausch & Lomb GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as Ophthalmic strabismus scissors, reusable.
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- Sklar® — Sklar Corporation · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4058935-000000-AC | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Bausch & Lomb GmbH
- EUDAMED SRN
- DE-MF-000009142
Sources (2)
- EUDAMED aa2a9377-5724-4730-aaed-72ba84c5edd4 61 fields · synced Jun 18, 2026
- FDA UDI 26e16e56-8dfd-4e95-8b88-0190c2d7c5ef 32 fields · synced May 30, 2026