Fixed Ang 30 Deg Dk 3.0/3.3mm Trap

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name: FIXED ANG 30 DEG DK 3.0/3.3MM TRAP FDA UDI
Generic Name: Ophthalmic knife, reusable FDA UDI
Device Name: FIXED ANG 30 DEG DK 3.0/3.3MM TRAP FDA UDI
Model / Reference: AE-8139 FDA UDI
Description: FIXED ANG 30 DEG DK 3.0/3.3MM TRAP FDA UDI

Identifiers

Catalog Number: AE-8139 FDA UDI
Primary DI / UDI-DI: 00841668141427 FDA UDI
FDA Product Code: HNN FDA UDI
GMDN Term: Ophthalmic knife, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 3 Millimeter FDA UDI
Width — 3.3 Millimeter FDA UDI

Category: Ophthalmic knife, reusable

Fixed Ang 30 Deg Dk 3.0/3.3mm Trap by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic knife, reusable.

MICRO FEATHER OPHTHALMIC SCALPEL with aluminum handle — FEATHER SAFETY RAZOR CO., LTD. · Class I
Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
Mastel Precision Surgical Instruments, Inc. — MASTEL SURGICAL INC. · Class I
Mastel Precision Surgical Instruments, Inc. — MASTEL SURGICAL INC. · Class I
Walcott Rx Products — Walcott Rx Product Inc · Class I
MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
Wexler Surgical, Inc. — Wexler Surgical, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Katena Products, Inc.

Sources (1)

FDA UDI 2dafd674-aa98-47fb-9a8d-a23cd05c7a1f 36 fields · synced Jun 12, 2026