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Hysteroscope Seal Caps

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Hysteroscope Seal Caps FDA UDI
Generic Name
Rigid optical laparoscope FDA UDI
Device Name
SEAL CAP OPERATIVE LAPAROSCOPE FDA UDI
Model / Reference
7205561 FDA UDI
Description
SEAL CAP OPERATIVE LAPAROSCOPE FDA UDI

Identifiers

Catalog Number
7205561 FDA UDI
Primary DI / UDI-DI
03596010465962 FDA UDI
510(k) Number
K980604 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid optical laparoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical laparoscope

Hysteroscope Seal Caps by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical laparoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI f79ae8cd-a964-4633-88bb-6c537f6642db 36 fields · synced Jun 8, 2026