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Forceps

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
FORCEPS FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Device Name
BABY ADSON, CURVED FDA UDI
Model / Reference
13-421-18-07 FDA UDI
Description
BABY ADSON, CURVED FDA UDI

Identifiers

Primary DI / UDI-DI
00888118019394 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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: Surgical soft-tissue manipulation forceps, scissors-like, reusable

At KLS-Martin L.P., we offer a range of medical instruments designed for precise and effective surgical procedures. Our FORCEPS device is a hand-held, manual instrument suitable for grasping, manipulating, dissecting, and/or clamping soft-tissues in various surgical specialties, including cardiovascular regulation.

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, scissors-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI e5750939-2086-4de0-8fa1-ad9232e589d1 35 fields · synced Jul 31, 2026