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Titanium Cooley Neonatal Clamp

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
TITANIUM COOLEY NEONATAL CLAMP FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Device Name
TITANIUM COOLEY NEONATAL CLAMP RIGHT ANGLED SHANK FDA UDI
Model / Reference
2605-174D FDA UDI
Description
TITANIUM COOLEY NEONATAL CLAMP RIGHT ANGLED SHANK FDA UDI

Identifiers

Primary DI / UDI-DI
B0992605174D0 FDA UDI
510(k) Number
K092544 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 4.75 Inch FDA UDI

Titanium Cooley Neonatal Clamp by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K092544 also covers:

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 4dfdccfb-d729-4dc1-926f-d339ad826f60 37 fields · synced Jun 8, 2026