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Surgicount

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SURGICOUNT FDA UDI
Generic Name
Electronic surgical sponge-counter FDA UDI
Device Name
+ EMR/QBL APPLICATION FDA UDI
Model / Reference
0694-002-100 FDA UDI
Description
+ EMR/QBL APPLICATION FDA UDI

Identifiers

Catalog Number
0694-002-100 FDA UDI
Primary DI / UDI-DI
07613327568981 FDA UDI
FDA Product Code
JQP FDA UDI
GMDN Term
Electronic surgical sponge-counter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2100 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electronic surgical sponge-counter

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

Similar devices

Also classified as Electronic surgical sponge-counter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 68059722-49cc-4e01-ac24-b02c5628485d 35 fields · synced May 29, 2026