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EndoWrist

FDA UDI

Class II (US FDA UDI)

by Intuitive Surgical, Inc.

Identity

Trade Name
EndoWrist FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
STAPLER 30 RELOAD GREEN FDA UDI
Model / Reference
48630G FDA UDI
Description
STAPLER 30 RELOAD GREEN FDA UDI

Identifiers

Primary DI / UDI-DI
00886874112847 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Surgical staple loading unit, non-cutting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Depth — 4.3 Millimeter FDA UDI

Category: Surgical staple loading unit, non-cutting

EndoWrist by Intuitive Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical staple loading unit, non-cutting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8d0d89e9-7393-43d3-aa89-d650977cceba 34 fields · synced Jun 9, 2026