← Back to catalogue

Solos

FDA UDI

Class II (US FDA UDI)

by Solos Endoscopy, Inc.

Identity

Trade Name
SOLOS FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
10mm Spoon Forcep, Auto Closure Handle FDA UDI
Model / Reference
GU1540 FDA UDI
Description
10mm Spoon Forcep, Auto Closure Handle FDA UDI

Identifiers

Primary DI / UDI-DI
00862311000434 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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 endoscopic tissue manipulation forceps, reusable

Solos by Solos Endoscopy, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Solos Endoscopy, Inc.

Sources (1)

  • FDA UDI 2fac4960-7cb1-42fe-b7fe-fa9db5d89d69 33 fields · synced Jun 1, 2026