FDA.reportPublic FDA data

V. Mueller

Primary DI
00724995316280
Brand
V. Mueller
Company
STERIS Deutschland GmbH
Model
OP0910001
Catalog number
OP0910001
Device description
V. Mueller GILLS-COLIBRI FORCEPS VERY DELICATE TIPS, FLAT FENESTRATED HANDLE OVERALL LENGTH 3 inches 7.6CM
Published
2026-10-27
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
HNRForceps, ophthalmic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HNRForceps, OphthalmicOphthalmic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10885403092428PreviousGS10
00724995316280PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088540309242810885403092428
00724995316280007249953162807249953162800724995316280

GMDN Terms#

Term, Definition table
TermDefinition
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusableA hand-held manual surgical instrument designed to facilitate the grasping, manipulation, or clamping of, and/or removal of foreign bodies from, ophthalmic soft-tissues (ocular tissues, eyelids), and may be pointed for capsulorhexis. It has a conventional (self-opening) or reverse-action (self-closing) tweezers-like design with variously designed tips, whereby the blades are designed to be opened/closed by squeezing between the fingers (i.e., without ring handles); it is not probe-like in design (i.e., not cannulated). It is typically made of metal, available in various sizes, and may have carbide inserts at the working end. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)548-4873xx@xx.xx

Regulatory Flags#

DUNS number
537625100
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00724995264468Snowden-Pencer3206003206002026-10-27
00724995264475Snowden-Pencer3206103206102026-10-27
00724995264482Snowden-Pencer3206203206202026-10-27
00724995264499Snowden-Pencer3206303206302026-10-27
00724995264505Snowden-Pencer3206403206402026-10-27
00724995264512Snowden-Pencer3207003207002026-10-27
00724995264529Snowden-Pencer3207013207012026-10-27
00724995264536Snowden-Pencer3207033207032026-10-27
00724995264543Snowden-Pencer3207053207052026-10-27
00724995264550Snowden-Pencer3207063207062026-10-27
00724995264567Snowden-Pencer3207083207082026-10-27
00724995264574Snowden-Pencer3207093207092026-10-27
00724995264581Snowden-Pencer3207103207102026-10-27
00724995264598Snowden-Pencer3207113207112026-10-27
00724995264604Snowden-Pencer3207123207122026-10-27
00724995264611Snowden-Pencer3207143207142026-10-27
00724995264628Snowden-Pencer3207203207202026-10-27
00724995264635Snowden-Pencer3207213207212026-10-27
00724995264642Snowden-Pencer3207503207502026-10-27
00724995264659Snowden-Pencer3207513207512026-10-27

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
07612717072169FINESSE REFLEXAlcon Laboratories, Inc.HNR2026-10-28
07612717072176FINESSE REFLEXAlcon Laboratories, Inc.HNR2026-10-28
07612717072190FINESSE REFLEXAlcon Laboratories, Inc.HNR2026-10-28
B382SD902769010Surgical DirectSurgical Direct, Inc.HNR2026-10-28
00724995266707Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266714Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266721Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266738Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266745Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266769Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266776Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00724995266783Snowden-PencerSTERIS Deutschland GmbHHNR2026-10-27
00190776437039MillenniumAvalign Technologies, Inc.HNR2026-10-23
00190776437046MillenniumAvalign Technologies, Inc.HNR2026-10-23
00190776437053MillenniumAvalign Technologies, Inc.HNR2026-10-23
00190776435721MillenniumAvalign Technologies, Inc.HNR2026-10-21
00190776435318MillenniumAvalign Technologies, Inc.HNR2026-10-19
G346EA32C0Epsilon USAEPSILON EYE CARE PRIVATE LIMITEDHNR2026-10-16
00190776434885MillenniumAvalign Technologies, Inc.HNR2026-10-14
00190776434984MillenniumAvalign Technologies, Inc.HNR2026-10-14
00192896123939Bishop Harmon Tissue ForcepsSONTEC INSTRUMENTS, INC.HNR2026-10-14
G346EA41VSS0Epsilon USAEPSILON EYE CARE PRIVATE LIMITEDHNR2026-10-14
00757770602506Bausch + LombBausch & Lomb IncorporatedHNR2026-10-09
00190776436209MillenniumAvalign Technologies, Inc.HNR2026-10-08
00190776433734MillenniumAvalign Technologies, Inc.HNR2026-10-07
00190776436155MillenniumAvalign Technologies, Inc.HNR2026-10-07
0081748902541323ga DEX™ Morris ILM ForcepsKATALYST SURGICAL LLCHNR2026-10-07
0084009620260127ga DEX™ Yoneda Super Grip ForcepsKATALYST SURGICAL LLCHNR2026-10-07
0084009620360823ga DEX™ Yoneda Super Grip ForcepsKATALYST SURGICAL LLCHNR2026-10-07
0084009620361525ga DEX™ Yoneda Super Grip ForcepsKATALYST SURGICAL LLCHNR2026-10-07