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Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Device Name
Hemostat Kelly 5-1/2" Curved FDA UDI
Model / Reference
1008381 FDA UDI
Description
Hemostat Kelly 5-1/2" Curved FDA UDI

Identifiers

Catalog Number
1008381 FDA UDI
Primary DI / UDI-DI
00304040022436 FDA UDI
FDA Product Code
HRQ FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Henry Schein's Hemostat Kelly 5-1/2" Curved instrument is a reusable, hand-held forceps used for soft-tissue manipulation during general surgery, plastic surgery, and other procedures. It features a curved blade and ring handles that allow for precise grasping and manipulation of tissues.

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
Henry Schein, Inc.

Sources (1)

  • FDA UDI 191931e6-d6e1-46c3-91f2-9e2a3b1e5629 34 fields · synced Jul 25, 2026