← Back to catalogue

Visitec

FDA UDI

Class II (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Visitec FDA UDI
Generic Name
Surgical tissue/fluid collection bag, non-sterile FDA UDI
Device Name
Fluid Collection Bag with Wick FDA UDI
Model / Reference
585701 FDA UDI
Description
Fluid Collection Bag with Wick FDA UDI

Identifiers

Primary DI / UDI-DI
30886158106372 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Surgical tissue/fluid collection bag, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Surgical tissue/fluid collection bag, non-sterile

Visitec by Beaver-Visitec International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical tissue/fluid collection bag, non-sterile.

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
Beaver-Visitec International, Inc.

Sources (1)

  • FDA UDI 8354a854-ee38-4f5d-ab3b-702d11a3e520 35 fields · synced May 29, 2026