National Hospital Packaging

FDA UDI

Class I (US FDA UDI)

by Surgi-Pak, Inc.

Identity

Trade Name: NATIONAL HOSPITAL PACKAGING FDA UDI
Generic Name: Tubular support bandage, non-latex, single-use FDA UDI
Device Name: TUBULAR RETENTION NETTING, SIZE 2, 36IN, 1/PKG, STRL FDA UDI
Model / Reference: 28-002 FDA UDI
Description: TUBULAR RETENTION NETTING, SIZE 2, 36IN, 1/PKG, STRL FDA UDI

Identifiers

Catalog Number: 28-002 FDA UDI
Primary DI / UDI-DI: 00817213022879 FDA UDI
FDA Product Code: FQM FDA UDI
GMDN Term: Tubular support bandage, non-latex, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tubular support bandage, non-latex, single-use

National Hospital Packaging by Surgi-Pak, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Tubular support bandage, non-latex, single-use.

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Juzo Bandaging Supplies — JULIUS ZORN, INC. · Class I
Juzo Bandaging Supplies — JULIUS ZORN, INC. · Class I
FLEXIGRIP TUBULAR BNDG SIZE K — BIRD & CRONIN, LLC · Class I
Juzo Bandaging Supplies — JULIUS ZORN, INC. · Class I
Juzo Bandaging Supplies — JULIUS ZORN, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Surgi-Pak, Inc.

Sources (1)

FDA UDI a07b58d7-cc8f-45df-ac6d-b9a9aad4e01b 35 fields · synced May 30, 2026