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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Uterine elevator FDA UDI
Device Name
Heaney Hysterectomy Retractor, BW 28mm x 82mm, OL 190mm (7 1/2") FDA UDI
Model / Reference
IPN017705 FDA UDI
Description
Heaney Hysterectomy Retractor, BW 28mm x 82mm, OL 190mm (7 1/2") FDA UDI

Identifiers

Catalog Number
P15951 FDA UDI
Primary DI / UDI-DI
14026704726148 FDA UDI
FDA Product Code
HCZ FDA UDI
GMDN Term
Uterine elevator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 28 Millimeter FDA UDI
Length — 190 Millimeter FDA UDI
Width — 82 Millimeter FDA UDI

Category: Uterine elevator

Pilling by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uterine elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 5c478a43-723f-4137-a33c-c8dc5bbc3860 36 fields · synced May 30, 2026