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Citec

FDA UDI

Class II (US FDA UDI)

by Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd.

Identity

Trade Name
CITEC FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Polyp trap, single chamber, non sterile, single use only. FDA UDI
Model / Reference
CIT-PT-01S FDA UDI
Description
Polyp trap, single chamber, non sterile, single use only. FDA UDI

Identifiers

Primary DI / UDI-DI
06975238202561 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical suction system collection container, single-use

Citec by Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd.

Sources (1)

  • FDA UDI 77d30808-ec91-4819-be03-5d076fc003e2 33 fields · synced May 30, 2026