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Tennant Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
TENNANT FORCEPS FDA UDI
Generic Name
Ophthalmic surgical device handling forceps, reusable FDA UDI
Device Name
TENNANT FORCEPS WITH TYING PLATFORM DELICATE STRAIGHT SMOOTH TIP ROUND HANDLE TITANIUM FDA UDI
Model / Reference
T14-5560 FDA UDI
Description
TENNANT FORCEPS WITH TYING PLATFORM DELICATE STRAIGHT SMOOTH TIP ROUND HANDLE TITANIUM FDA UDI

Identifiers

Catalog Number
T14-5560 FDA UDI
Primary DI / UDI-DI
00192896016569 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic surgical device handling forceps, 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

Category: Ophthalmic surgical device handling forceps, reusable

Tennant Forceps by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical device handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI ed381001-75b8-4d3c-a304-ff10de8f02e7 35 fields · synced May 30, 2026