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Triton Canister System

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Triton Canister System FDA UDI
Generic Name
Blood loss estimation canister insert/label FDA UDI
Device Name
MediVac CRD 3L v2 Scanning Label and Insert (PN 11032 and PN 11012) FDA UDI
Model / Reference
PN 11035 FDA UDI
Description
MediVac CRD 3L v2 Scanning Label and Insert (PN 11032 and PN 11012) FDA UDI

Identifiers

Primary DI / UDI-DI
00859506006135 FDA UDI
510(k) Number
K142801 FDA UDI
FDA Product Code
PBZ FDA UDI
GMDN Term
Blood loss estimation canister insert/label FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2750 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood loss estimation canister insert/label

Triton Canister System by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood loss estimation canister insert/label.

Cleared under the same submission

K142801 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 3507efcd-f8fa-4d86-848d-ab9745d589ac 34 fields · synced Jun 1, 2026