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BandGrip® Micro-Anchor® Skin Closure

FDA UDI

Class I (US FDA UDI)

by Bandgrip Inc.

Identity

Trade Name
BandGrip® Micro-Anchor® Skin Closure FDA UDI
Generic Name
Skin-closure adhesive strip FDA UDI
Device Name
9 cm x 4 cm; w/ 2 Strips FDA UDI
Model / Reference
BG1001 FDA UDI
Description
9 cm x 4 cm; w/ 2 Strips FDA UDI

Identifiers

Catalog Number
BG1001 FDA UDI
Primary DI / UDI-DI
00850010207070 FDA UDI
FDA Product Code
FZQ FDA UDI
GDT FDA UDI
KGX FDA UDI
MKY FDA UDI
GMDN Term
Skin-closure adhesive strip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4320 FDA UDI
878.4760 FDA UDI
880.5240 FDA UDI
Commercial Distribution
Not 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 9 Centimeter FDA UDI
Width — 4 Centimeter FDA UDI

BandGrip® Micro-Anchor® Skin Closure by Bandgrip Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bandgrip Inc.

Sources (1)

  • FDA UDI e05b3450-2371-44a6-b288-67a3ac425d3b 37 fields · synced May 30, 2026