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Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Spring-loaded pneumoperitoneum needle, reprocessed FDA UDI
Device Name
Cotton Rolls Wrapped Sterile FDA UDI
Model / Reference
5703768 FDA UDI
Description
Cotton Rolls Wrapped Sterile FDA UDI

Identifiers

Catalog Number
5703768 FDA UDI
Primary DI / UDI-DI
10304040184858 FDA UDI
FDA Product Code
EFN FDA UDI
GMDN Term
Spring-loaded pneumoperitoneum needle, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6050 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Spring-loaded pneumoperitoneum needle, reprocessed

Henry Schein by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spring-loaded pneumoperitoneum needle, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Henry Schein, Inc.

Sources (1)

  • FDA UDI e738cf6e-1b33-4c8f-997e-f32fd7f95ad8 34 fields · synced Jun 6, 2026