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US Tip Pack, 20GA, Flared, SH

FDA UDI

Class II (US FDA UDI)

by Medical Technical Products, Inc

Identity

Trade Name
US Tip Pack, 20GA, Flared, SH FDA UDI
Generic Name
Ophthalmic surgical procedure kit, non-medicated, reusable FDA UDI
Model / Reference
23-9025 FDA UDI

Identifiers

Primary DI / UDI-DI
00850039020223 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgical procedure kit, non-medicated, reusable

US Tip Pack, 20GA, Flared, SH by Medical Technical Products, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Technical Products, Inc

Sources (1)

  • FDA UDI f944879b-720d-4e3c-b3f7-7574e18207e1 33 fields · synced Jun 8, 2026