Laryngoscopy Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name: Laryngoscopy Forceps FDA UDI
Generic Name: Flexible endoscopic biopsy forceps, reusable FDA UDI
Device Name: Laryngoscopy Forceps Conical Tube Tip Angled Up FDA UDI
Model / Reference: 1301-272 FDA UDI
Description: Laryngoscopy Forceps Conical Tube Tip Angled Up FDA UDI

Identifiers

Catalog Number: 1301-272 FDA UDI
Primary DI / UDI-DI: 00192896058538 FDA UDI
FDA Product Code: KAE FDA UDI
GMDN Term: Flexible endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 9 Inch FDA UDI

Category: Flexible endoscopic biopsy forceps, reusable

Laryngoscopy Forceps by Sontec Instruments, 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: Sontec Instruments, Inc.

Sources (1)

FDA UDI 44eb0cc5-ed29-4485-bb57-275d8c3c1f44 36 fields · synced Jun 8, 2026