← Back to catalogue

SurgiCount

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SurgiCount FDA UDI
Generic Name
Surgical sponge-counting rack FDA UDI
Device Name
+ Stand 3.0 FDA UDI
Model / Reference
0894002001 FDA UDI
Description
+ Stand 3.0 FDA UDI

Identifiers

Catalog Number
0894-002-001 FDA UDI
Primary DI / UDI-DI
07613327625882 FDA UDI
FDA Product Code
LWH FDA UDI
GMDN Term
Surgical sponge-counting rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical sponge-counting rack

SurgiCount by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical sponge-counting rack.

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
Stryker Corp.

Sources (1)

  • FDA UDI d6190bf7-37e7-49bd-8697-59a9abf2c933 36 fields · synced May 30, 2026