East Coast Surgical Instruments

FDA UDI

Class II (US FDA UDI)

by East Coast Surgical Inc.

Identity

Trade Name: East Coast Surgical Instruments FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: Filter For Insufflation Tubing W/ 6" Pig-Tail FDA UDI
Model / Reference: 14-7102 FDA UDI
Description: Filter For Insufflation Tubing W/ 6" Pig-Tail FDA UDI

Identifiers

Primary DI / UDI-DI: 00850837007105 FDA UDI
FDA Product Code: FCX FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic insufflation tubing set, single-use

East Coast Surgical Instruments by East Coast Surgical Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: East Coast Surgical Inc.

Sources (1)

FDA UDI 7e51de84-771f-4028-9a76-5e64d69c9e32 33 fields · synced May 30, 2026