16205-01050 +2 more models

FDA UDI

Class I (US FDA UDI)

by Hankil Tech Medical Co., Ltd.

Identity

Trade Name: 16205-01050; 16205-01110; 60-025 FDA UDI
Generic Name: Surgical depth gauge, reusable FDA UDI
Device Name: Depth Gauge for ilyac, 110mm FDA UDI
Model / Reference: 16205-01110 FDA UDI
Description: Depth Gauge for ilyac, 110mm FDA UDI

Identifiers

Catalog Number: 16205-01110 FDA UDI
Primary DI / UDI-DI: 08809452519205 FDA UDI
FDA Product Code: HTJ FDA UDI
GMDN Term: Surgical depth gauge, reusable FDA UDI
Models / Variants: 16205-01050 FDA UDI
16205-01110 FDA UDI
60-025 FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4300 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

Yes

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Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 110 Millimeter FDA UDI

Category: Surgical depth gauge, reusable

16205-01050 +2 more models by Hankil Tech Medical Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — 3 models — 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: Hankil Tech Medical Co., Ltd.

Sources (1)

FDA UDI 79fc3030-fbde-4e09-84ea-f168130cadc0 36 fields · synced Jun 8, 2026