Identity
- Trade Name
- KITAHARA ROTATABLE GLAUCOMA PUNCH FDA UDI
- Generic Name
- Corneoscleral punch FDA UDI
- Device Name
- KITAHARA ROTATABLE GLAUCOMA PUNCH FDA UDI
- Model / Reference
- AE-8304 FDA UDI
- Description
- KITAHARA ROTATABLE GLAUCOMA PUNCH FDA UDI
Identifiers
- Catalog Number
- AE-8304 FDA UDI
- Primary DI / UDI-DI
- 00841668142790 FDA UDI
- FDA Product Code
- HNJ FDA UDI
- GMDN Term
- Corneoscleral punch 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Corneoscleral punch
Kitahara Rotatable Glaucoma Punch by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Corneoscleral punch.
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- ATLAS — ATLAS CERRAHİ ALETLER LTD. ŞTİ. · Class I
- V. Mueller — STERIS 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
- Katena Products, Inc.
Sources (1)
- FDA UDI 47fb3c6e-0076-4ac5-b7d7-ccfeeba768a8 35 fields · synced Jun 12, 2026