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Hemovac® Wound Drainage System

FDA UDI

Class I (US FDA UDI)

by Zimmer Orthopaedic Surgical Products

Identity

Trade Name
Hemovac® Wound Drainage System FDA UDI
Generic Name
Closed-wound/centesis drainage receptacle FDA UDI
Device Name
450ml Bag Packaged FDA UDI
Model / Reference
00-1500-050-10 FDA UDI
Description
450ml Bag Packaged FDA UDI

Identifiers

Catalog Number
00-1500-050-10 FDA UDI
Primary DI / UDI-DI
00889024370234 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Closed-wound/centesis drainage receptacle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 400 Milliliter FDA UDI

Hemovac® Wound Drainage System by Zimmer Orthopaedic Surgical Products — Class I — 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

Sources (1)

  • FDA UDI 119429eb-8a0d-4724-9224-c8b3eac61b41 37 fields · synced May 31, 2026