Identity
- Trade Name
- 20ga Dex Tips™ NanoTapered™ Hybrid Forceps FDA UDI
- Generic Name
- Ophthalmic tissue forceps, single-use FDA UDI
- Device Name
- Box of 5, 20ga Dex Tips™ NanoTapered™ Hybrid Forceps FDA UDI
- Model / Reference
- CVF4007-20 FDA UDI
- Description
- Box of 5, 20ga Dex Tips™ NanoTapered™ Hybrid Forceps FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817489022764 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic tissue forceps, 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ophthalmic tissue forceps, single-use
20ga Dex Tips™ NanoTapered™ Hybrid Forceps by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic tissue forceps, single-use.
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
- Katalyst Surgical, Llc
Sources (1)
- FDA UDI 339c5b94-794b-49f6-a37b-a3fda4db8a28 33 fields · synced May 30, 2026