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Triton

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
TRITON FDA UDI
Generic Name
Blood loss estimation canister insert/label FDA UDI
Device Name
TRITON 3L CANISTER INSERT KIT FDA UDI
Model / Reference
FG-12022 FDA UDI
Description
TRITON 3L CANISTER INSERT KIT FDA UDI

Identifiers

Catalog Number
FG-12022 FDA UDI
Primary DI / UDI-DI
00859506006258 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

No

FDA UDI

Category: Blood loss estimation canister insert/label

Triton 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 88c566db-f201-4f8f-b323-fd240f48a326 35 fields · synced Jun 8, 2026