← Back to catalogue

Resp-O2 Reusable Outer Suction Canister, 1500 cc, Wall Mount

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Reusable Outer Suction Canister, 1500 cc, Wall Mount FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Model / Reference
32251 FDA UDI

Identifiers

Primary DI / UDI-DI
00840117321564 FDA UDI
FDA Product Code
KDQ 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical suction system collection container, single-use

Resp-O2 Reusable Outer Suction Canister, 1500 cc, Wall Mount by Dynarex Corp. — 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

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

Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI d9a8656a-17fc-4141-b42b-cfc204d74250 32 fields · synced Jun 8, 2026