Snowden-Pencer 88-9348
GUDID 10885403154836
DIAMOND-LINE KNOT PUSHER OPEN END 5MM, 32CM DELICATE
CAREFUSION 2200, INC
Suture knot pusher, reusable| Primary Device ID | 10885403154836 |
| NIH Device Record Key | 94ad7b05-48e0-4e22-be4a-640064686545 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Snowden-Pencer |
| Version Model Number | 88-9348 |
| Catalog Number | 88-9348 |
| Company DUNS | 832696038 |
| Company Name | CAREFUSION 2200, INC |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)323-9088 |
| gmb-MedSpec-CustService@carefusion.com | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10885403154836 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K930667
FDA Product Code
| GCJ | Laparoscope, general & plastic surgery |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
[10885403154836]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-05-06 |
| Device Publish Date | 2016-09-23 |
On-Brand Devices [Snowden-Pencer]
| 70885403154609 | HASSON "S" RETRACTOR 1 PAIR, LARGE |
| 70885403154593 | HASSON "S" RETRACTOR 1 PAIR, SMALL |
| 70885403048236 | ENDOPLASTIC DISSECTOR CVD SHAFT-STRAIGHT TIP-5MM ESU 14.5" (36.5CM) 2 PER PACKAGE (X 2) |
| 70885403048229 | ENDOPLASTIC DISSECTOR STRAIGHT SHAFT-ANG TIP-5MM ESU 14.5" (36.5CM) 2 PER PACKAGE (X 2) |
| 70885403048205 | ENDOPLASTIC DISSECTOR CVD RT SHAFT-STR TIP-5MM ESU 14.5" (36.5CM) 2 PER PACKAGE (X 2) |
| 70885403048199 | ENDOPLASTIC DISSECTOR CVD LEFT SHAFT-STR TIP-5MM ESU 14.5" (36.5CM) 2 PER PACKAGE (X 2) |
| 10885403220098 | SLIDELOCK GRASPER TAKE-APART, SINGLE ACTION 45 CM, 5MM, 22MM JAW, RETRACT, INSUL SHFT, ROT, RACH |
| 10885403219979 | SLIDELOCK GRASPER TAKE-APART, SINGLE ACTION 45 CM, 5MM, 22MM JAW, RETRACTION, INSERT |
| 10885403152504 | ELEVATOR MITCHELLS TRIMMER 17CM (6 5/8") |
| 10885403220081 | SLIDELOCK GRASPER TAKE-APART, SINGLE ACTION 37CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, RACHETED |
| 10885403220067 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, SINGLE ACTION 45CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, |
| 10885403220050 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, |
| 10885403220012 | SLIDELOCK DORSEY GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 30MM JAW INSERT |
| 10885403220005 | SLIDELOCK DORSEY GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 30MM JAW INSERT |
| 10885403219986 | SLIDELOCK GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 22MM JAW INSERT |
| 10885403219962 | SLIDELOCK GRASPER TAKE-APART, SINGLE ACTION 37CM, 5MM, 22MM JAW RETRACTION, INSERT |
| 10885403219948 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, SINGLE ACTION 37CM, 5MM, 22MM JAW INSERT |
| 10885403219931 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 22MM JAW INSERT |
| 10885403219573 | SLIDELOCK GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, RACHETED |
| 10885403155055 | GOLD-LINE GRASPER MCKERNAN FUNDUS 5MM, 32CM, RATCHETED |
| 10885403154829 | OPEN-END KNOT PUSHER 5MM HANDLE, STANDARD FOR 5-0 & LARGER SUTURE WORKING LENGTH 12-1/2" (32CM) |
| 10885403220128 | SLIDELOCK TENACULUM GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 33MM JAW INSUL SHFT, ROTATION, |
| 10885403220111 | SLIDELOCK DORSEY GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 30MM JAW INSUL SHFT, ROTATION, RAC |
| 10885403220104 | SLIDELOCK DORSEY GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 30MM JAW INSUL SHFT, ROTATION, RAC |
| 10885403220074 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, SINGLE ACTION 37CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, |
| 10885403220043 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, |
| 10885403220029 | SLIDELOCK TENACULUM GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 33MM JAW INSERT |
| 10885403219993 | SLIDELOCK GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 22MM JAW INSERT |
| 10885403219924 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, DOUBLE ACTION 37CM, 5MM, 22MM JAW INSERT |
| 10885403219580 | SLIDELOCK RERACTION GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 22MM JAW INSUL SHFT, ROTATION, |
| 10885403155048 | GOLD-LINE GRASPER MCKERNAN ALLIS 5MM, 32CM, RATCHETED |
| 70885403465118 | INCISION PICK 15MM REPLACEMENT BLADE PACK OF 5 5/PK (X 5) |
| 10885403220135 | SLIDELOCK TENACULUM GRASPER TAKE-APART, DOUBLE ACTION 45CM, 5MM, 33MM JAW INSUL SHFT, ROTATION, |
| 10885403220036 | SLIDELOCK TENACULUM GRASPER TAKE-APART, SINGLE ACTION 45CM, 5MM, 33MM JAW INSERT |
| 10885403219955 | SLIDELOCK ATRAUMATIC GRASPER TAKE-APART, SINGLE ACTION 45CM, 5MM, 22MM JAW INSERT |
| 10885403154836 | DIAMOND-LINE KNOT PUSHER OPEN END 5MM, 32CM DELICATE |
| 10885403155093 | ENDOSCOPIC MEASURING PROBE GRADUATED, ARTICULATING SHAFT 5MM 38CM |
| 10885403152283 | MCKISSOCK KEYHOLE MARKER 45MM ACCURACY +/- 1.0MM |
| 10885403152276 | MCKISSOCK KEYHOLE MARKER 42MM ACCURACY +/- 1.0MM |
| 10885403152269 | MCKISSOCK KEYHOLE MARKER 38MM ACCURACY +/- 1.0MM |
| 10885403152030 | TEBBETTS SKIN HOOK SELF-RETAINING 15CM (6"), 11MM DOUBLE HOOK |
| 10885403151996 | TEBBETTS SKIN HOOK SELF-RETAINING 15CM (6"), SINGLE HOOK |
| 10885403152047 | TEBBETTS SKIN HOOK SELF-RETAINING, WITH BALL END 15CM (6"), 13MM DOUBLE HOOK |
| 10885403152023 | TEBBETTS SKIN HOOK SELF-RETAINING 15CM (6"), 8MM DOUBLE HOOK |
| 10885403152016 | TEBBETTS SKIN HOOK SELF-RETAINING 15CM (6"), 6MM DOUBLE HOOK |
| 10885403152009 | TEBBETTS SKIN HOOK SELF-RETAINING 15CM (6"), 2MM DOUBLE HOOK |
| 10885403151989 | HOOKS LIGHT WEIGHT STRAIGHT SKIN 15CM (6"), DELICATE |
| 10885403151958 | HOOKS CONVERSE SKIN 15CM (6") |
| 10885403141188 | BARSKY DOUBLE SKIN HOOK 5MM DIAMETER OVERALL LENGTH 5-1/2" (14CM) |
| 10885403148460 | DIAMOND-SEREDGES SCISSORS BOSTWICK-MAYO, SERRATED 23CM (9"), STRAIGHT |
Trademark Results [Snowden-Pencer]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SNOWDEN-PENCER 73646911 1471925 Live/Registered |
SNOWDEN-PENCER, INC. 1987-02-27 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.