Disp Peribulbar Needle 25ga 7/8" 10/Box

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name: DISP PERIBULBAR NEEDLE 25GA 7/8" 10/BOX FDA UDI
Generic Name: Ophthalmic needle, single-use FDA UDI
Device Name: DISP PERIBULBAR NEEDLE 25GA 7/8" 10/BOX FDA UDI
Model / Reference: AS-7068 FDA UDI
Description: DISP PERIBULBAR NEEDLE 25GA 7/8" 10/BOX FDA UDI

Identifiers

Catalog Number: AS-7068 FDA UDI
Primary DI / UDI-DI: 00841668111925 FDA UDI
FDA Product Code: GAA FDA UDI
GMDN Term: Ophthalmic needle, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Category: Ophthalmic needle, single-use

Disp Peribulbar Needle 25ga 7/8" 10/Box by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 9f55e2ef-eb30-4e0e-9796-33c52c9413ac 35 fields · synced Jun 12, 2026