Identity

Trade Name
Suction Kit FDA UDI
Generic Name
Secretion suction kit FDA UDI
Device Name
This kit contains: 1 RES023 Suction Canister, 1 RES024 Suction Tubing Connector - 3.5in, 1 BF3812 Final Bacteria Filter - 3/8in x 1/2in, 1 RES028 Rubber Suction Elbow. FDA UDI
Model / Reference
RES026-ENT FDA UDI
Description
This kit contains: 1 RES023 Suction Canister, 1 RES024 Suction Tubing Connector - 3.5in, 1 BF3812 Final Bacteria Filter - 3/8in x 1/2in, 1 RES028 Rubber Suction Elbow. FDA UDI

Identifiers

Catalog Number
RES026-ENT FDA UDI
Primary DI / UDI-DI
00848530062323 FDA UDI
GMDN Term
Secretion suction kit FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Secretion suction kit

Suction Kit by SUNSET HEALTHCARE SOLUTIONS, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secretion suction kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4fcbd154-fd80-42f5-8893-106372f2543e 35 fields · synced May 30, 2026