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Henry Schein

FDA UDI

Class II (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Skin-approximation adhesive FDA UDI
Device Name
Topical Skin Adhesive Blue FDA UDI
Model / Reference
1126111 FDA UDI
Description
Topical Skin Adhesive Blue FDA UDI

Identifiers

Catalog Number
1126111 FDA UDI
Primary DI / UDI-DI
00304040006412 FDA UDI
FDA Product Code
MPN FDA UDI
GMDN Term
Skin-approximation adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Peracetic Acid FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Total Volume — 0.5 Milliliter FDA UDI

Category: Skin-approximation adhesive

Henry Schein by Henry Schein, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-approximation adhesive.

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 eaf1d4c6-0dae-4ef8-b38f-b703f0ef85d8 36 fields · synced Jun 1, 2026