← Back to catalogue

Black Micro Artery Clamp Pair

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BLACK MICRO ARTERY CLAMP PAIR FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Device Name
BLACK MICRO ARTERY CLAMP PAIR FDA UDI
Model / Reference
2100-HD-DAB FDA UDI
Description
BLACK MICRO ARTERY CLAMP PAIR FDA UDI

Identifiers

Primary DI / UDI-DI
B0992100HDDAB0 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

No

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 — 24 Millimeter FDA UDI

Black Micro Artery Clamp Pair 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI 381678aa-943a-403a-af0f-4a3802c4d3b6 37 fields · synced May 31, 2026