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Hayden Medical

FDA UDI

Class I (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name
Hayden Medical FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Green Tissue Forceps 4" (10cm), T-shape, 12mm wide 19x20 teeth, with lock FDA UDI
Model / Reference
120-895 FDA UDI
Description
Green Tissue Forceps 4" (10cm), T-shape, 12mm wide 19x20 teeth, with lock FDA UDI

Identifiers

Catalog Number
120-895 FDA UDI
Primary DI / UDI-DI
00840319720400 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Green Tissue Forceps 4" (10cm), T-shape, 12mm wide 19x20 teeth, with lock. These reusable, handheld medical devices facilitate the grasping, manipulation, or clamping of and/or removal of foreign bodies from ophthalmic soft-tissues.

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hayden Medical Inc

Sources (1)

  • FDA UDI 9b1b12b6-91f8-4eff-8c0a-aa04bee7832d 35 fields · synced Jul 23, 2026