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Valtrac

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Valtrac FDA UDI
Generic Name
Gastrointestinal anastomosis coupler, non-bioabsorbable FDA UDI
Device Name
Biofragmentable Anastomotic Ring FDA UDI
Model / Reference
8886809200 FDA UDI
Description
Biofragmentable Anastomotic Ring FDA UDI

Identifiers

Primary DI / UDI-DI
10884521052505 FDA UDI
510(k) Number
K931056 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Gastrointestinal anastomosis coupler, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Dimensions & Sizes

Size
Outer Diameter — 34 Millimeter FDA UDI
Height — 2.5 Millimeter FDA UDI

Valtrac by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 8fc71c96-773b-4e47-9a78-4f3db36f8d41 38 fields · synced Jun 1, 2026