Katena K20-6000
by Katena Products, Inc. United States GUDID
Product code PZG
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841668123331 | Date2 Mar 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Katena
- Generic Name
- Ophthalmic surgical procedure kit, non-medicated, single-use
- Model / Ref / Catalog
- K20-6000
- Primary DI / UDI-DI
- 00841668123331
- FDA Product Code
- PZG
- GMDN Term
- Ophthalmic surgical procedure kit, non-medicated, single-use
- Device Class
- Class I
- Regulation Number
- 886.4350
- Commercial Distribution
- In Commercial Distribution
Properties & raw data
Show properties, registry sources and raw records
Other properties (7)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 176e8889-f35d-4016-9dae-fa33fce1c53e