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Half Pipe

FDA UDI

Class I (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
Half Pipe FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
Half Pipe®, long FDA UDI
Model / Reference
28728LH FDA UDI
Description
Half Pipe®, long FDA UDI

Identifiers

Primary DI / UDI-DI
04048551008133 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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: Endoscope sheath, reusable

Half Pipe by Karl Storz GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope sheath, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI d9e0ee46-d762-4ad9-a3e4-622e2e8a4646 33 fields · synced Jun 8, 2026