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Orthopaedic Suction Set

FDA UDI

Class II (US FDA UDI)

by Gcmedica Enterprise Ltd.(wuxi)

Identity

Trade Name
Orthopaedic Suction Set FDA UDI
Generic Name
General-purpose surgical suction system, vacuum FDA UDI
Device Name
Sterile, single use, easyflow filtered suction system, for orthopaedic surgery. FDA UDI
Model / Reference
AEEFS1111 FDA UDI
Description
Sterile, single use, easyflow filtered suction system, for orthopaedic surgery. FDA UDI

Identifiers

Primary DI / UDI-DI
06970754496159 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
General-purpose surgical suction system, vacuum 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose surgical suction system, vacuum

Orthopaedic Suction Set by Gcmedica Enterprise Ltd.(wuxi) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical suction system, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gcmedica Enterprise Ltd.(wuxi)

Sources (1)

  • FDA UDI 4e36d995-c23f-43c0-bbfe-a2eda6f0a879 33 fields · synced Jun 8, 2026