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Rhapso

FDA UDI

Class II (US FDA UDI)

by Applied Medical Technology, Inc.

Identity

Trade Name
RHAPSO FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
RHAPSO Suture Passer (Curved Needle, Pouched) FDA UDI
Model / Reference
ESD110-C-07 FDA UDI
Description
RHAPSO Suture Passer (Curved Needle, Pouched) FDA UDI

Identifiers

Catalog Number
ESD110-C-07, SD110-C-07-101, SD110-C-07-105 FDA UDI
Primary DI / UDI-DI
00842071149420 FDA UDI
510(k) Number
K241111 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Suturing unit, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suturing unit, single-use

Rhapso by Applied Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3cbf3d68-4342-41e3-a9c4-e8dd5d828cf0 36 fields · synced Jun 9, 2026