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MICTEC Biopsy Forceps

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICTEC Biopsy Forceps FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
MICTEC Biopsy Forceps 20 Degree Curved Down Y-Grip Without Ratchet With Cleaning Flush Port 2.7 Millimeter Diameter FDA UDI
Model / Reference
27976-36-020 FDA UDI
Description
MICTEC Biopsy Forceps 20 Degree Curved Down Y-Grip Without Ratchet With Cleaning Flush Port 2.7 Millimeter Diameter FDA UDI

Identifiers

Catalog Number
27976-36-020 FDA UDI
Primary DI / UDI-DI
00192896120297 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 200 Millimeter FDA UDI

Category: Rigid endoscopic biopsy forceps, reusable

MICTEC Biopsy Forceps by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic biopsy forceps, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7c57cae3-7544-4ed9-8c34-6bea725afedf 37 fields · synced May 30, 2026