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Endo-Misc

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Endo-Misc FDA UDI
Generic Name
Rigid endoscopic grasping forceps, reusable FDA UDI
Device Name
EXTENDED HIP GRASPER FDA UDI
Model / Reference
E0015761-1 FDA UDI
Description
EXTENDED HIP GRASPER FDA UDI

Identifiers

Catalog Number
E0015761-1 FDA UDI
Primary DI / UDI-DI
00885556706428 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Rigid endoscopic grasping forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

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 endoscopic grasping forceps, reusable

Endo-Misc by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic grasping forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3cf6f6c0-adaf-4e74-8c47-c9cbceba2313 35 fields · synced Jun 8, 2026