← Back to catalogue

Rescuer 7000-AD Replacement Suction Canister kit

FDA UDI

Class I (US FDA UDI)

by B.L.S. Systems Limited

Identity

Trade Name
Rescuer 7000-AD Replacement Suction Canister kit FDA UDI
Generic Name
Emergency airway clearance suction pump, manual FDA UDI
Device Name
Replacement canister kit and catheters for 7000-MVP FDA UDI
Model / Reference
7000-AD FDA UDI
Description
Replacement canister kit and catheters for 7000-MVP FDA UDI

Identifiers

Catalog Number
7000-AD FDA UDI
Primary DI / UDI-DI
B0027000AD0 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Emergency airway clearance suction pump, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 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

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: Emergency airway clearance suction pump, manual

Rescuer 7000-AD Replacement Suction Canister kit by B.L.S. Systems Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction pump, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
B.L.S. Systems Limited

Sources (1)

  • FDA UDI 5c5a6968-71a6-46d9-9da5-24f60ef3e9c8 36 fields · synced May 31, 2026