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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
BLADE MCCULLOCH WIDE MUSCLE 5CM FDA UDI
Model / Reference
IPN019648 FDA UDI
Description
BLADE MCCULLOCH WIDE MUSCLE 5CM FDA UDI

Identifiers

Catalog Number
P22251 FDA UDI
Primary DI / UDI-DI
34026704653875 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Self-retaining surgical retractor, reusable

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

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5fe6cc23-d62c-4988-bb64-d70e6360edcb 35 fields · synced May 30, 2026