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STILLE Scissors

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Scissors FDA UDI
Generic Name
Blepharoplasty scissors FDA UDI
Device Name
STILLE BLEPHAROPLASTY SUPERCUT SCISSORS curved 9.5 cm 3.75 in FDA UDI
Model / Reference
101-8019-1 FDA UDI
Description
STILLE BLEPHAROPLASTY SUPERCUT SCISSORS curved 9.5 cm 3.75 in FDA UDI

Identifiers

Catalog Number
101-8019-1 FDA UDI
Primary DI / UDI-DI
07332339200145 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Blepharoplasty scissors FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 9.5 Centimeter FDA UDI

Category: Blepharoplasty scissors

STILLE Scissors by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blepharoplasty scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI e2970dba-f0c1-41f1-88ae-593c0e328552 36 fields · synced May 30, 2026