Identity
- Trade Name
- Tissue Holder FDA UDI
- Generic Name
- Corneal resection holder, single-use FDA UDI
- Device Name
- BARRON ARTIFICIAL ANTERIOR CHAMBER FDA UDI
- Model / Reference
- K20-2125 FDA UDI
- Description
- BARRON ARTIFICIAL ANTERIOR CHAMBER FDA UDI
Identifiers
- Catalog Number
- K20-2125 FDA UDI
- Primary DI / UDI-DI
- 00841668112847 FDA UDI
- FDA Product Code
- HRH FDA UDI
- GMDN Term
- Corneal resection holder, 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Corneal resection holder, single-use
Tissue Holder by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Corneal resection holder, single-use.
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- Bausch + Lomb — Bausch & Lomb Incorporated · U
- Coronet — Network Medical Products, Ltd. · Class I
- Tissue Holder — Katena Products, Inc. · 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 134597a5-6854-4d96-b809-5b84b03ef7ee 35 fields · synced Jun 12, 2026