Identity

Trade Name
Suction Kit FDA UDI
Generic Name
Secretion suction kit FDA UDI
Device Name
This Kit Contains: 1 RES023S Suction Canister 800cc, 1 RES028 Rubber Suction Elbor Connector, 1 RES024M Silicone Tubing Connector 4.5in. FDA UDI
Model / Reference
INH003SUCTKIT FDA UDI
Description
This Kit Contains: 1 RES023S Suction Canister 800cc, 1 RES028 Rubber Suction Elbor Connector, 1 RES024M Silicone Tubing Connector 4.5in. FDA UDI

Identifiers

Catalog Number
INH003SUCTKIT FDA UDI
Primary DI / UDI-DI
00848530089658 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 1d26eb02-abf0-40c5-8df0-839745cfe6a9 35 fields · synced May 31, 2026